Therapies based on control of regulatory t cell stability and function via a neuropilin-1:semaphorin axis

ABSTRACT

The invention is directed to treatment of cancer, infections and various inflammatory and autoimmune conditions by affecting regulatory T cell stability and function via a Neuropilin-1:Semaphorin axis. The present invention satisfies this and other needs by demonstrating that the regulatory T cell (Treg)-restricted neuropilin-1 (Nrp 1) interacts with the cell surface ligand semaphorin-4a (Sema4a) (e.g., on conventional T cells (Tconv), conventional dendritic cells (cDCs), and/or plasmacytoid dendritic cells (pDCs)) to potentiate reg function and enhance their survival at inflammatory sites.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of U.S. Provisional Patent Application No. 61/784,607, filed Mar. 14, 2013, U.S. Provisional Application No. 61/712,679, filed Oct. 11, 2012, and U.S. Provisional Application No. 61/711,193, filed Oct. 8, 2012, all of which are incorporated herein by reference in their entirety.

STATEMENT AS TO FEDERALLY SPONSORED RESEARCH

The United States Government has certain rights to this invention by virtue of funding reserved from Grant Nos. AI091977, AI039480 and AI098383 from the National Institutes of Health and NCI Comprehensive Cancer Center Support CORE grant CA21765.

FIELD OF THE INVENTION

The present invention is directed to treatment of cancer, infections and various inflammatory and autoimmune conditions by affecting regulatory T cell stability and function via a Neuropilin-1:Semaphorin axis.

BACKGROUND OF THE INVENTION

Regulatory T cells (Tregs) play a crucial role in preventing autoimmunity, limiting immunopathology and maintaining immune homeostasis¹. However, they also represent a major barrier to effective anti-tumor immunity and sterilizing immunity to chronic viral infections. This highlights the capacity of Tregs to shape and control a wide range of immune responses. Foxp3 is a master transcriptional regulator required for the development, maintenance and stability of Tregs^(2,3). Mice and humans with non-functional Foxp3 lack Tregs and develop a lethal systemic autoimmune condition, referred to as Scurfy in mice and IPEX in humans, highlighting the importance of Tregs in the maintenance of immune homeostasis^(2,3). Furthermore, a transcription factor quintet forms a redundant genetic switch to ‘lock-in’ the Treg transcriptional signature and enhance their stability⁴. Although some external factors, such as transforming growth factor-β (TGFβ), have been shown to maintain and/or enhance Foxp3 stability and function⁵, it is unknown if additional cell-extrinsic pathways or factors exist.

Tissue-resident Tregs are some of the first lymphoid cells to respond to an infection or inflammatory response, thereby limiting immune pathology^(6,7). Some environments, such as tumors and chronic infections, can be highly inflammatory and thus may require additional mechanisms or genetic programs to enhance the stability and function of Tregs in order to limit unintended inflammatory or autoimmune disease. Consequently there is considerable interest in identifying molecular pathways that control Treg stability and function as many immune-mediated diseases are characterized by either exacerbated or limited Treg function, and the adoptive transfer of Tregs for the treatment of a variety of diseases is being actively pursued in the clinic.

Treg stability versus plasticity has been a topic of considerable recent debate. Some studies have defined critical roles for lineage-specific transcription factors, such as T-bet, IRF4 and STAT3, in regulating specific types of T cell responses driven by the same transcription factors⁸⁻¹⁰. In contrast, others have suggested that a demonstrable proportion of Tregs differentiate in inflammatory sites into ‘ex-Tregs’ and gain effector function¹¹. The cell-extrinsic factors and molecular mechanisms by which Tregs alter their transcriptional profile to maintain their stability, regulate immunity in inflammatory sites and control these alternate cell fates remain obscure.

Neuropilin-1 (Nrp1; see, e.g., GenBank Accession Nos. NM 008737 (mouse) and NG 030328 (human) as well as various isoforms) is a membrane-bound coreceptor to a tyrosine kinase receptor for both vascular endothelial growth factor (VEGF) and class III semaphorin Sema3a. Nrp1 plays versatile roles in axon guidance, angiogenesis, cell survival, migration, and invasion¹⁵. Nrp1 induces axon growth cone collapse, preventing infiltration into privileged tissues and its genetic deletion in mice results in embryonic lethality¹⁶. Nrp1 has been also shown to interact platelet derived growth factor beta (PDGFβ) and transforming growth factor beta (TGFβ)^(17,18.) Nrp1 has been shown to be highly expressed in Tregs¹⁹⁻²¹. Although a role for Nrp1 in T cells has been implicated²², no role for Nrp1 in Tregs has been identified and it has been suggested that Nrp1 is not expressed on human Tregs²⁵.

SUMMARY OF THE INVENTION

As specified in the Background Section, there is a great need in the art to identify the molecular pathways that control Treg stability and function and use this understanding to develop novel therapeutics for the treatment of cancer, infections and various inflammatory and autoimmune conditions. The present invention satisfies this and other needs by demonstrating that the regulatory T cell (Treg)-restricted neuropilin-1 (Nrp1) interacts with the cell surface ligand semaphorin-4a (Sema4a) (e.g., on conventional T cells (Tconv), conventional dendritic cells (cDCs), and/or plasmacytoid dendritic cells (pDCs)) to potentiate Treg function and enhance their survival at inflammatory sites.

In one embodiment, the invention provides a method of inhibiting a function or decreasing stability of a regulatory T cell (Treg) comprising exposing said Treg to an inhibitor of neuropilin-1 (Nrp1):semaphorin axis in said Treg. In one embodiment, the inhibitor of Nrp1:semaphorin axis inhibits interaction between a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) on a cell expressing such transmembrane semaphorin (e.g., a conventional T cell (Tconv), a conventional dendritic cell (cDC), or a plasmacytoid dendritic cell (pDC)) and Nrp1 on the Treg. In one embodiment, the inhibitor of Nrp1:semaphorin axis does not affect Nrp1-VEGF interaction in said Treg. In one embodiment, said Treg is in a subject (e.g., human) and the inhibitor of Nrp1:semaphorin axis is administered to the subject. In one embodiment, the subject has a cancer (e.g., melanoma or glioblastoma). In another embodiment, the subject has an infection in which Tregs are blocking sterilizing immunity (e.g., a chronic infection). In one embodiment, the inhibitor of Nrp1:semaphorin axis is an antibody (e.g., an antibody which does not affect Nrp1-VEGF interaction in said Treg). In another embodiment, the inhibitor of Nip 1:semaphorin axis is a semaphorin molecule (e.g., a soluble version of a transmembrane semaphorin protein [e.g., a class IV semaphorin such as, e.g., Sema4a] or a fragment or a derivative or an analog thereof [including various fusion molecules such as, e.g., a Sema4a extracellular domain fused to Fc region of IgG1 at the C-terminus], wherein said soluble version of a transmembrane semaphorin protein, fragment, derivative or analog is capable of binding with high affinity and specificity to Nrp1 on Treg without potentiating Nrp1:semaphorin axis in said Treg). In yet another embodiment, the inhibitor of Nrp1:semaphorin axis is a soluble extracellular domain of Nrp1 protein or a fragment or a derivative or an analog thereof, wherein said soluble extracellular domain of Nrp1 protein, fragment, derivative or analog is capable of binding with high affinity and specificity to a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) thereby preventing said transmembrane semaphorin from potentiating Nrp1:semaphorin axis in said Treg. In a further embodiment, the inhibitor of Nrp1:semaphorin axis inhibits expression of Nrp1 protein in the Treg (e.g., is an siRNA or an antisense oligonucleotide). In a further embodiment, the inhibitor of Nrp1:semaphorin axis prevents Nrp1 from engaging with its downstream signaling pathway(s). In one specific embodiment, the inhibitor of Nrp1:semaphorin axis inhibits a signaling pathway between the cytoplasmic domain of Nrp1 protein comprising the C-terminal amino acid sequence SEA (C-terminal PDZ domain-binding motif) and PTEN protein; such inhibitor can be, e.g., a peptide or a small molecule or a fragment of Nrp1 protein comprising all or part of its cytoplasmic domain comprising the C-terminal amino acid sequence SEA or a derivative or an analog thereof. In one specific embodiment, the inhibitor of Nrp1:semaphorin axis is a small molecule.

In a separate embodiment, the invention provides a method of enhancing a function or increasing stability of a regulatory T cell (Treg) comprising exposing said Treg to an agonist of neuropilin-1 (Nrp1):semaphorin axis in said Treg. In one embodiment, the agonist of Nrp1:semaphorin axis enhances interaction between a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) on a cell expressing such transmembrane semaphorin (e.g., a conventional T cell (Tconv), a conventional dendritic cell (cDC), or a plasmacytoid dendritic cell (pDC)) and Nrp1 on the Treg. In one embodiment, the agonist of Nrp1:semaphorin axis is administered to the Treg in vitro. In one embodiment, the Treg is extracted from a subject (e.g., human), is expanded ex vivo in the presence of the agonist of Nrp1-semaphorin interaction and then (i) is reintroduced back into the subject or (ii) is administered to a different subject. In one embodiment, the subject receiving expanded Tregs has an autoimmune or an inflammatory disease. In another embodiment, the Treg is in a subject (e.g., human) and the agonist of Nrp1:semaphorin axis is administered to the subject. In one embodiment, the subject has an autoimmune or an inflammatory disease. In one embodiment, the agonist of Nrp1:semaphorin axis is a semaphorin molecule (e.g., a multimerized semaphorin molecule and/or a semaphorin molecule immobilized on a surface or a bead). In one embodiment, the semaphorin molecule is a class IV semaphorin (e.g., Sema4a) or a fragment or a derivative or an analog thereof. In one embodiment, the agonist of Nrp1:semaphorin axis is an antibody. In another embodiment, the agonist of Nrp1:semaphorin axis is a small molecule. In yet another embodiment, the agonist of Nrp1:semaphorin axis enhances Nrp1 expression in the Treg. In a further embodiment, the agonist of Nrp1:semaphorin axis enhances Nrp1 engagement with its downstream signaling pathway(s).

In a separate embodiment, the invention provides a method of treating a disease in a subject (e.g., human) in need thereof, the method comprising inhibiting neuropilin-1 (Nrp1):semaphorin axis in regulatory T cells (Tregs) of the subject. In one embodiment, the method comprises inhibiting interaction between a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) on cells expressing such transmembrane semaphorin (e.g., conventional T cells (Tconv), conventional dendritic cells (cDCs), and/or plasmacytoid dendritic cells (pDCs)) and Nrp1 on the Tregs of the subject. In one embodiment, the disease is a cancer (e.g., melanoma or glioblastoma). In another embodiment, the disease is an infection in which Tregs are blocking sterilizing immunity (e.g., a chronic infection). In one embodiment, the method comprises administering to the subject a therapeutically effective amount of an inhibitor of neuropilin-1 (Nrp1):semaphorin axis in Tregs of the subject. In one embodiment, the inhibitor of Nrp1:semaphorin axis is an antibody (e.g., an antibody which does not affect Nrp1-VEGF interaction in the Tregs of the subject). In another embodiment, the inhibitor of Nrp1:semaphorin axis is a semaphorin molecule (e.g., a soluble version of a transmembrane semaphorin protein [e.g., a class IV semaphorin such as, e.g., Sema4a] or a fragment or a derivative or an analog thereof [including various fusion molecules such as, e.g., a Sema4a extracellular domain fused to Fc region of IgG1 at the C-terminus], wherein said soluble version of a transmembrane semaphorin protein, fragment, derivative or analog is capable of binding with high affinity and specificity to Nrp1 on Tregs without potentiating Nrp1:semaphorin axis in said Tregs). In yet another embodiment, the inhibitor of Nrp1:semaphorin axis is a soluble extracellular domain of Nrp1 protein or a fragment or a derivative or an analog thereof, wherein said soluble extracellular domain of Nrp1 protein, fragment, derivative or analog is capable of binding with high affinity and specificity to a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) thereby preventing said transmembrane semaphorin from potentiating Nrp1:semaphorin axis in the Tregs of the subject. In a further embodiment, the inhibitor of Nrp1:semaphorin axis inhibits expression of Nrp1 protein in the Tregs of the subject (e.g., is an siRNA or an antisense oligonucleotide). In a further embodiment, the inhibitor of Nrp1:semaphorin axis prevents Nrp1 from engaging with its downstream signaling pathway(s). In one specific embodiment, the inhibitor of Nrp1:semaphorin axis inhibits a signaling pathway between the cytoplasmic domain of Nrp1 protein comprising the C-terminal amino acid sequence SEA (C-terminal PDZ domain-binding motif) and PTEN protein; such inhibitor can be, e.g., a peptide or a small molecule or a fragment of Nrp1 protein comprising all or part of its cytoplasmic domain comprising the C-terminal amino acid sequence SEA or a derivative or an analog thereof. In one specific embodiment, the inhibitor of Nrp1:semaphorin axis is a small molecule. In another embodiment, the method further comprises administering to the subject an additional immunomodulatory treatment (e.g., a therapeutic vaccine, a checkpoint inhibitor or an activator). In yet another embodiment, the method further comprises administering to the subject a chemotherapy or a radiation therapy (for treatment of cancers) or administering an antibiotic (for treatment of infections).

In a separate embodiment, the invention provides a method of treating a disease in a subject (e.g., human) in need thereof, the method comprising activating neuropilin-1 (Nrp1):semaphorin axis in regulatory T cells (Tregs) of the subject. In one embodiment, the method comprises enhancing interaction between a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) on cells expressing such transmembrane semaphorin (e.g., conventional T cells (Tconv), conventional dendritic cells (cDCs), and/or plasmacytoid dendritic cells (pDCs)) and Nrp1 on the Tregs of the subject. In one embodiment, the subject has an autoimmune or inflammatory disease. In one embodiment, the method comprises administering to the subject a therapeutically effective amount of an agonist of neuropilin-1 (Nrp1):semaphorin axis in Tregs of the subject. In one embodiment, the agonist of Nrp1:semaphorin axis is a semaphorin molecule (e.g., a multimerized semaphorin molecule and/or a semaphorin molecule immobilized on a surface or a bead). In one embodiment, the semaphorin molecule is a class IV semaphorin (e.g., Sema4a) or a fragment or a derivative or an analog thereof. In one embodiment, the agonist of Nrp1:semaphorin axis is an antibody. In another embodiment, the agonist of Nrp1:semaphorin axis is a small molecule. In yet another embodiment, the agonist of Nrp1:semaphorin axis enhances Nrp1 expression in the Tregs of the subject. In a further embodiment, the agonist of Nrp1:semaphorin axis enhances Nrp1 engagement with its downstream signaling pathway(s). In another embodiment, the method further comprises administering to the subject another therapy which enhances Tregs or blocks inflammation.

In a separate embodiment, the invention provides a method for enhancing the efficacy of a vaccine (e.g., a vaccine for treating or preventing cancer or infection) in a subject (e.g., human), the method comprising administering to the subject an effective amount of an inhibitor of neuropilin-1 (Nrp1):semaphorin axis in Tregs of the subject. In one embodiment, the inhibitor of Nrp1:semaphorin axis is an antibody (e.g., an antibody which does not affect Nrp1-VEGF interaction in the Tregs of the subject). In another embodiment, the inhibitor of Nrp1:semaphorin axis is a semaphorin molecule (e.g., a soluble version of a transmembrane semaphorin protein [e.g., a class IV semaphorin such as, e.g., Sema4a] or a fragment or a derivative or an analog thereof [including various fusion molecules such as, e.g., a Sema4a extracellular domain fused to Fc region of IgG1 at the C-terminus], wherein said soluble version of a transmembrane semaphorin protein, fragment, derivative or analog is capable of binding with high affinity and specificity to Nrp1 on Tregs without potentiating Nrp1:semaphorin axis in said Tregs). In yet another embodiment, the inhibitor of Nrp1:semaphorin axis is a soluble extracellular domain of Nrp1 protein or a fragment or a derivative or an analog thereof, wherein said soluble extracellular domain of Nrp1 protein, fragment, derivative or analog is capable of binding with high affinity and specificity to a transmembrane semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) thereby preventing said transmembrane semaphorin from potentiating Nrp1:semaphorin axis in the Tregs of the subject. In a further embodiment, the inhibitor of Nrp1:semaphorin axis inhibits expression of Nrp1 protein in the Tregs of the subject (e.g., is an siRNA or an antisense oligonucleotide). In a further embodiment, the inhibitor of Nrp1:semaphorin axis prevents Nrp1 from engaging with its downstream signaling pathway(s). In one specific embodiment, the inhibitor of Nrp1:semaphorin axis inhibits a signaling pathway between the cytoplasmic domain of Nrp1 protein comprising the C-terminal amino acid sequence SEA (C-terminal PDZ domain-binding motif) and PTEN protein; such inhibitor can be, e.g., a peptide or a small molecule or a fragment of Nrp1 protein comprising all or part of its cytoplasmic domain comprising the C-terminal amino acid sequence SEA or a derivative or an analog thereof. In one specific embodiment, the inhibitor of Nrp1:semaphorin axis is a small molecule. In one embodiment of the method, the inhibitor of Nrp1:semaphorin axis is administered to the subject before the vaccine is administered to the subject. In another embodiment of the method, the inhibitor of Nrp1:semaphorin axis is administered to the subject together with the vaccine.

In a separate embodiment, the invention provides an isolated antibody which inhibits neuropilin-1 (Nrp1):semaphorin (e.g., a class IV semaphorin such as, e.g., Sema4a) interaction on a regulatory T cell (Treg).

These and other aspects of the present invention will be apparent to those of ordinary skill in the art in the following description, claims and drawings.

BRIEF DESCRIPTION OF THE DRAWINGS

FIGS. 1A-E demonstrate that Semaphorin 4a potentiates regulatory T cell function. A, Transwell suppression assay of Tconv stimulated with anti-CD3/anti-CD28 coated beads in the bottom well when regulatory T cells (Tregs) are stimulated in the top well in the presence of the indicated cell types. For some conditions, the coculture cell population was fixed prior to Treg stimulation. B, Transwell suppression assay in which neutralizing antibodies to semaphorin-4a (Sema4a) were included. C, CD4⁺ or CD8⁺ Tconv were mock transfected or transfected with scrambled siRNA or Sema4a siRNA and then boosting potential assessed in a Transwell suppression assay. D, Transwell suppression assay in which Treg monocultures were stimulated with beads coated with mouse IgG1 or Sema4a-Ig in the top well. E, Transwell suppression assay in which fixed dendritic cells sorted direct ex vivo as well as neutralizing antibodies to semaphorin-4a (Sema4a) were included. Results represent the mean of five [A, D] or three [B, C, E] experiments. *, p<0.05, **, p<0.01, ***, p<0.001 by unpaired t-test.

FIGS. 2A-I demonstrate that Nrp1 acts as the ligand for Semaphorin-4a on Tregs. A, Transwell suppression assay in which Tconv:Treg cocultures were stimulated in the presence of an neutralizing anti-Nrp1 antibody or its isotype control. B, Transwell suppression assay with Foxp3^(Cre) or Nrp1^(f/f) Foxp3^(Cre) Tregs. C, Transwell suppression assay using WT, IL-10^(−/−), or Ebi3^(−/−) Treg in the top well cocultured with Sema4a-Ig beads and WT or dnTGFbRII Tconv in the bottom well. D, Transwell suppression assay using Tregs cultured with Sema4a-Ig beads in the presence or absence of neutralizing antibodies to IL-10 and IL-35. E, Tabulation of flow cytometric analysis of Annexin V and 7-AAD staining in Treg 48 hours after stimulation with anti-CD3/CD28 coated beads, IL-2, and either isotype or Sema4a-Ig coated beads. F, NRP-1 expression on human Tconv or Treg cells sorted from umbilical cord blood and culture with anti-CD3, anti-CD28, and IL-2 for the indicated times. G, Transwell suppression assay in which 8-day-expanded human Treg were cultured with either IgG or hSema4a-Ig coated beads, or with fixed autologous human Teff in the presence or absence of blocking antibodies to NRP1. H, ELISA-based binding assay in which plates coated with recombinant mNrp1 were incubated with Sema4a-Ig or mouse IgG1, in the presence of isotype controls, anti-Nrp1, or anti-Sema4a. Sema4a-Ig or mouse IgG1 was detected using an anti-isotype antibody. I, Transwell suppression assay in which Tconv:Treg cocultures were stimulated in the presence of an neutralizing anti-Nrp1 antibody or its isotype control. Results represent the mean of three [A, D-F, H, I] or five [B, C, G] experiments. *, p<0.05, **, p<0.01, ***, p<0.001 by unpaired t-test.

FIGS. 3A-C demonstrate that Nrp1-deficient Tregs prevent the autoimmune disease of Foxp3-deficient animals. A, Survival curve of Foxp3⁻ male mice that received no injection or 1×10⁶ Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) Treg at 1-2 days of age. B, Clinical scores at 5 weeks of mice treated as in A. C, Histological scores of of liver, lung, and ear pinna (combined) from mice treated as in a. Results represent three independent experiments. **, p<0.01 by one-way ANOVA [A], **, p<0.001 by unpaired t-test [B-C], ns, not significant, p>0.05.

FIGS. 4A-J demonstrate that Nrp1-deficient Tregs fail to suppress anti-tumor responses or highly inflammatory colitis. A, Tumor growth curve (top) and survival plot (bottom) of Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) mice receiving 1.25×10⁵ MC38 melanoma cells s.c. B, As in A, but mice received 1.25×10⁵ EL4 thymoma i.d. C, As in A, but mice received 1.25×10⁵ B16 melanoma i.d. D, Lung metastasis counts from Foxp3^(C) or Nrp1^(f/f)Foxp3^(Cre) mice injected with 2.5-10×10⁵ B16 cells i.v. 17-20 days earlier. E, Tabulation of flow cytometric analysis of tumor-infiltrating lymphocytes from Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) mice injected i.d. with B16 18 days earlier. F, Tumor growth curve of C57/BL6 mice receiving 1.25×10⁵ B16 melanoma i.d. When tumors were palpable (day 5, indicated by arrow), mice began receiving injections of anti-Nrp1 or its isotype control (400 μg initial dose, 200 μg every 3 days). G, Histology of large intestine of Rag2^(−/−) mice that had or had not received 4×10⁵ CD4⁺CD45RB⁺CD25⁻ cells to induce colitis, then PBS or 1×10⁶ Tregs from Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) mice after colitis was detected. H, Sema4a expression of various immune cells in ndLN, dLN, or TIL. I, Tumor growth curve of C57/BL6 mice receiving 1.25×10⁵ B16 melanoma i.d. concomitant with injections of isotype control, anti-Sema4a, or anti-Nrp1 (100 μg) twice weekly. J, Tumor growth curve as in g except mice received Sema4a-Ig twice weekly. Results represent the mean of five (A-C, I-J n=10-25 mice), three (D,E,F,H n=8-17 mice), or four (G) experiments. *, p<0.05, **, p<0.01, ***, p<0.001, by (A-C, I-J) one-way ANOVA or (D-F,H) unpaired t-test.

FIGS. 5 A-D demonstrate that ligation of Nrp1 by Sema4a promotes Treg stability through the modulation of Akt-mTOR signaling. A, Flow cytometric analysis of Akt signaling in Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) Tregs. Flow cytometrically-purified Tregs were left resting or stimulated with anti-CD3/anti-CD28 beads overnight in the presence of beads coated with Sema4a-Ig or isotype control. B, TIRF microscopic analysis of Akt activation in immunologic synapses (IS) of Tregs stimulated 20 min on a lipid bilayer coated with anti-TCR antibodies in the presence or absence of Sema4a-Ig. C, Immunoprecipitation analysis of Nrp1 using Tregs expanded with PMA and ionomycin for 3 days, followed by a 5-7 day expansion in 500 U/mL rhIL-2, serum starved for 3 h, then stimulated as indicated for 3 hours prior to IP. D, Transwell suppression assay using Foxp3^(Cre) or Pten^(f/f)Foxp3^(Cre) Tregs. Results are the mean of three (A, B, D) or represent at least three experiments (C). *, p<0.05, ** p<0.01 by unpaired t-test.

FIGS. 6A-D demonstrate that neuropilin restrains IS Akt activation via PTEN. A, Tabulation of pAkt occurrence in IS from FIG. 5B. B, TIRF microscopy of IS activation of Akt and pTyr in Foxp3^(Cre) or Nrp1^(f/f) Foxp3^(Cre) Treg purified flow cytometrically and then stimulated on a lipid bilayer containing anti-TCR and either IgG or Sema4a-Ig. C, TIRF microscopy of IS recruitment of neuropilin and activation of Akt in Foxp3^(Cre) or Pten^(f/f)Foxp3^(Cre) Treg purified flow cytometrically and then stimulated for 20 minutes on a lipid bilayer containing anti-TCR and either IgG or Sema4a-Ig. D, Tabulation of pAkt occurrence in IS from C. Results are representative of three [A-B] or two [C-D] independent experiments. *** p<0.001 by one-way ANOVA.

FIGS. 7A-I demonstrate that tumor-infiltrating Treg bear a signature similar to Sema4a:Nrp1 ligation. A, Akt activation of tumor-infiltrating Treg. Tumor bearing Foxp3^(Cre) or Nrp1f/fFoxp3Cre mice were sacrificed on day 12 and ndLN and TIL were harvested. After gradient centrifugation cells were immediately fixed and stained for Akt activation. Shaded histogram indicates isotype control. Results are tabulated beneath normalized to isotype control staining Helios (B), IRF4/RORγt (C), Ki67/BrdU (D), cleaved caspase-3 (E) Bcl2 (F) IL-10 (G) CD73 (H) and LAG-3 (I) staining from ndLN, dLN, or TIL from tumor-bearing Foxp3Cre or Nrp1f/fFoxp3Cre mice. For Ki67/BrdU analysis, animals were injected with BrdU 14 h prior to harvest. For IL-10 staining, cells were restimulated with PMA and ionomycin for 16 h in the presence of a protein transport inhibitor. Results represent the mean of three independent experiments. * p<0.05, ** p<0.01, *** p<0.001 by paired t-test [A, n=7] or unpaired t-test [B-I, n=8-25].

FIG. 8 shows schematically how neuropilin maintains Treg stability. Naïve Treg maintain low Akt activation, which promotes their quiescence through the activity of factors like Foxos and KLF2 (left). Upon activation, Tregs stimulated in the absence of Sema4a:Nrp1 have high activation of Akt, which promotes the nuclear exclusion of Foxos, leading to loss of Treg stability (center). Nrp1 ligation via Sema4a restrains Akt activation via recruitment of PTEN, inhibiting the nuclear exclusion of Foxos (right). This promotes a genetic program associated with stability and increased Treg function.

DETAILED DESCRIPTION OF THE INVENTION

The present invention is based on an unexpected observation that that the immune cell surface ligand semaphorin-4a (Sema4a) on conventional murine and human T cells and the regulatory T cell (Treg)-restricted receptor neuropilin-1 (Nrp1) interact to potentiate Treg function and enhance their survival. Mice with a Treg-restricted deletion of Nrp1 exhibit limited tumor-induced tolerance, and thus substantial resistance to certain tumors, yet do not develop any autoimmune or inflammatory manifestations. As specified in the Examples section, below, Nrp1 blockade also has therapeutic efficacy against pre-existing tumors. Nrp1 is recruited to the immunological synapse (IS) and represses Akt activity via phosphatase and tensin homolog (PTEN), which facilitate Foxo nuclear translocation. This induces a transcriptional program that promotes Treg stability, survival and function while repressing the induction of lineage-specific transcription factors. Thus, Nrp1 ligation enforces Treg stability and function in highly inflammatory sites but is dispensable for the maintenance of immune homeostasis, highlighting inhibition of Nrp1-semaphorin axis as a immunotherapeutic target in cancer and infections, while its potentiation as a target in treating autoimmunity and inflammation. Blocking Nrp1-semaphorin interaction could limit Treg function in tumors but not elsewhere enhancing anti-tumor activity without adverse side effects. This can provide effective cancer treatment and prevention both at very early stages of tumor development and during late stages, including metastasis. Similar approaches could be efficacious in any other diseases where Tregs pose a barrier (e.g., chronic infections in which Tregs are blocking sterilizing immunity, such as, e.g., HCV, HBV, HIV infections, etc.) and may enhance vaccination. On the other hand, enhancing Nrp1-semaphorin interaction would increase Treg function in diseases where they fail (e.g., autoimmune and inflammatory conditions). In connection with enhancing Nrp1-semaphorin interaction to increase Treg function, also disclosed herein is adoptive therapy approach, wherein patient's Tregs are expanded ex vivo in the presence of an agonist of Nip 1-semaphorin interaction and then are reintroduced back into the same patient or are administered to a different patient.

DEFINITIONS

The terms “Treg” or “regulatory T cell” refer to CD4⁺ T cells that suppresses CD4⁺CD25⁻ and CD8⁺ T cell proliferation and/or effector function, or that otherwise down-modulate an immune response. Notably, Treg may down-regulate immune responses mediated by Natural Killer cells, Natural Killer T cells as well as other immune cells. In a preferred embodiment, Tregs of the invention are Foxp3⁺.

The terms “regulatory T cell function” or “a function of Treg” are used interchangeably to refer to any biological function of a Treg that results in a reduction in CD4⁺CD25⁻ or CD8⁺ T cell proliferation or a reduction in an effector T cell-mediated immune response. Treg function can be measured via techniques established in the art. Non-limiting examples of useful in vitro assays for measuring Treg function include Transwell suppression assay described in the Examples section, below, as well as, more generally, in vitro assays in which the target conventional T cells (Tconv) and Tregs purified from human peripheral blood or umbilical cord blood (or murine spleens or lymph nodes) are optionally activated by anti-CD3⁺ anti-CD28 coated beads (or antigen-presenting cells (APCs) such as, e.g., irradiated splenocytes or purified dendritic cells (DCs) or irradiated PBMCs) followed by in vitro detection of conventional T cell proliferation (e.g., by measuring incorporation of radioactive nucleotides (such as, e.g., [³H]-thymidine) or fluorescent nucleotides, or by Cayman Chemical MTT Cell Proliferation Assay Kit, or by monitoring the dilution of a green fluorochrome ester CFSE or Seminaphtharhodafluor (SNARF-1) dye by flow cytometry). Other common assays measure T cell cytokine responses. Useful in vivo assays of Treg function include assays in animal models of diseases in which Tregs play an important role, including, e.g., (1) homeostasis model (using naïve homeostatically expanding CD4⁺ T cells as target cells that are primarily suppressed by Tregs), (2) inflammatory bowel disease (IBD) recovery model (using Th1 T cells (Th17) as target cells that are primarily suppressed by Tregs), (3) experimental autoimmune encephalomyelitis (EAE) model (using Th17 and Th1 T cells as target cells that are primarily suppressed by Tregs), (4) B16 melanoma model (suppression of antitumor immunity) (using CD8⁺ T cells as target cells that are primarily suppressed by Tregs), (5) suppression of colon inflammation in adoptive transfer colitis where naïve CD4⁺CD45RB^(hi) Tconv cells are transferred into Rag1^(−/−) mice, and (6) Foxp3⁻ rescue model (using lymphocytes as target cells that are primarily suppressed by Tregs). According to one protocol, all of the models require mice for donor T cell populations as well as Rag1^(−/−) or Foxp3⁻ mice for recipients. For more details on various useful assays see, e.g., Collison and Vignali, In Vitro Treg Suppression Assays, Chapter 2 in Regulatory T Cells: Methods and Protocols, Methods in Molecular Biology, Kassiotis and Liston eds., Springer, 2011, 707:21-37; Workman et al., In Vivo Treg Suppression Assays, Chapter 9 in Regulatory T Cells: Methods and Protocols, Methods in Molecular Biology, Kassiotis and Liston eds., Springer, 2011, 119-156; Takahashi et al., Int. Immunol., 1998, 10:1969-1980; Thornton et al., J. Exp. Med., 1998, 188:287-296; Collison et al., J. Immunol., 2009, 182:6121-6128; Thornton and Shevach, J. Exp. Med., 1998, 188:287-296; Asseman et al., J. Exp. Med., 1999, 190:995-1004; Dieckmann et al., J. Exp. Med., 2001, 193:1303-1310; Belkaid, Nature Reviews, 2007, 7:875-888; Tang and Bluestone, Nature Immunology, 2008, 9:239-244; Bettini and Vignali, Curr. Opin. Immunol., 2009, 21:612-618; Dannull et al., J Clin Invest, 2005, 115(12):3623-33; Tsaknaridis, et al., J Neurosci Res., 2003, 74:296-308.

The term “neuropilin-1 (Nrp1):semaphorin axis of a regulatory T cell (Treg)” as used herein refers to the signaling pathway initiated by semaphorin (e.g., a semaphorin expressed by a cell such as, e.g., a conventional T cell, or a recombinant semaphorin), ligation of Nrp1, and the subsequent downstream signaling.

The terms “antagonist” or “inhibitor” in connection with Nrp1:semaphorin axis of Tregs are used interchangeably herein and refer to any agent that can (i) interfere with the productive ligation and/or crosslinking of semaphorin:Nrp1 or (ii) inhibit the immediate downstream signaling consequences of Nrp1 in Tregs. The inhibition of Nrp1:semaphorin interaction on Tregs can be assessed by any of the methods known in the art, including Transwell suppression assay described in the Examples section, below.

The terms “agonist” or “potentiator” in connection with Nrp1:semaphorin axis of Tregs are used interchangeably herein and refer to any agent that can (i) enhance interaction of Nrp1:semaphorin, or (ii) mimic semaphorin stimulation and Nrp1 signaling artificially to the Treg, or (iii) activate immediate downstream signaling consequences of Nrp1 in Tregs. The enhancement of Nrp1:semaphorin interaction on Tregs can be assessed by any of the methods known in the art, including the Transwell suppression assay described in the Examples section, below.

For therapeutic applications, the agonists and antagonists of the present invention can be used as pharmaceutical compositions and can be optionally combined with other agonists/antagonists of the invention or other therapeutic molecules.

The term “a semaphorin molecule” as used herein in connection with agonists of the Nrp1:semaphorin axis of Tregs encompasses transmembrane semaphorin molecules involved in interaction with Nrp1 on Tregs (e.g., Sema4a), various surface- and bead-immobilized versions of such molecules, as well as multimers, derivatives, mutants, analogs, and fragments of such molecules which can be used to enhance a function or increase stability of Tregs. Non-limiting examples of such agonist semaphorin molecules are discussed in more detail below and include, for example, IgM-derived semaphorin fusion proteins that assemble multimeric complexes incapable of fixing complement, that crosslink Nrp1 solubly.

The term “a semaphorin molecule” as used herein in connection with inhibitors of the Nrp1:semaphorin axis of Tregs encompasses soluble versions of transmembrane semaphorin molecules involved in interaction with Nrp1 on Tregs (e.g., Sema4a) as well as various derivatives, mutants, analogs, and fragments of such molecules (including various fusion molecules), which can be used to inhibit a function or decrease stability of Tregs. Non-limiting examples of such inhibitory semaphorin molecules are discussed in more detail below and include, for example, various soluble fragments of Sema4a and derivatives or analogs thereof which outcompete endogenous Sema4a for Nrp1 binding. In one specific embodiment, the inhibitory semaphorin molecule is Sema4a-Ig fusion protein, which is a fusion (at the C-terminus) between Sema4a extracellular domain (Met1-His683 fragment of GenBank Accession No. NP_(—)038686) and the Fc region of human or murine IgG1.

The term “analog” refers to a molecule that is not identical, but has analogous functional or structural features. For example, a polypeptide analog retains the biological activity of a corresponding naturally-occurring polypeptide, while having certain biochemical modifications that enhance the analog's function relative to a naturally occurring polypeptide. Such biochemical modifications could increase the analog's protease resistance, membrane permeability, or half-life, without altering, for example, ligand binding. An analog may include an unnatural amino acid.

The term “inflammation” as used herein refers to any excessive or undesirable immune response. The term “inflammatory disease” as used herein refers to any pathology associated with an excessive or an undesirable immune response.

The term “about” means within an acceptable error range for the particular value as determined by one of ordinary skill in the art, which will depend in part on how the value is measured or determined, i.e., the limitations of the measurement system. For example, “about” can mean within an acceptable standard deviation, per the practice in the art. Alternatively, “about” can mean a range of up to ±20%, preferably up to ±10%, more preferably up to ±5%, and more preferably still up to ±1% of a given value. Alternatively, particularly with respect to biological systems or processes, the term can mean within an order of magnitude, preferably within 2-fold, of a value. Where particular values are described in the application and claims, unless otherwise stated, the term “about” is implicit and in this context means within an acceptable error range for the particular value.

In the context of the present invention insofar as it relates to any of the disease conditions recited herein, the terms “treat”, “treatment”, and the like mean to relieve or alleviate at least one symptom associated with such condition, or to slow or reverse the progression of such condition. Within the meaning of the present invention, the term “treat” also denotes to arrest, delay the onset (i.e., the period prior to clinical manifestation of a disease) and/or reduce the risk of developing or worsening a disease. E.g., in connection with cancer the term “treat” may mean eliminate or reduce a patient's tumor burden, or prevent, delay or inhibit metastasis, etc.

As used herein the term “therapeutically effective” applied to dose or amount refers to that quantity of a compound or pharmaceutical composition that is sufficient to result in a desired activity upon administration to a subject in need thereof. Within the context of the present invention, the term “therapeutically effective” refers to that quantity of a compound (e.g., an antagonist or agonist of Nrp1:semaphorin axis of Tregs) or pharmaceutical composition containing such compound that is sufficient to delay the manifestation, arrest the progression, relieve or alleviate at least one symptom of a disorder treated by the methods of the present invention. Note that when a combination of active ingredients is administered the effective amount of the combination may or may not include amounts of each ingredient that would have been effective if administered individually.

The phrase “pharmaceutically acceptable”, as used in connection with compositions of the invention, refers to molecular entities and other ingredients of such compositions that are physiologically tolerable and do not typically produce untoward reactions when administered to a mammal (e.g., a human). Preferably, as used herein, the term “pharmaceutically acceptable” means approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia or other generally recognized pharmacopeia for use in mammals, and more particularly in humans.

As used herein, the term “subject” refers to any mammal. In a preferred embodiment, the subject is human.

As used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural references unless the context clearly dictates otherwise.

In accordance with the present invention there may be employed conventional molecular biology, microbiology, and recombinant DNA techniques within the skill of the art. Such techniques are explained fully in the literature. See, e.g., Sambrook, Fritsch & Maniatis, Molecular Cloning: A Laboratory Manual, Second Edition (1989) Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (herein “Sambrook et al., 1989”); DNA Cloning: A practical Approach, Volumes I and II (D. N. Glover ed. 1985); Oligonucleotide Synthesis (MJ. Gait ed. 1984); Nucleic Acid Hybridization (B. D. Hames & S. J. Higgins eds.(1985>>; Transcription and Translation (B. D. Hames & S. J. Higgins, eds. (1984>>; Animal Cell Culture (R. I. Freshney, ed. (1986>>; Immobilized Cells and Enzymes (IRL Press, (1986>>; B. Perbal, A practical Guide To Molecular Cloning (1984); F. M. Ausubel et al. (eds.), Current Protocols in Molecular Biology, John Wiley & Sons, Inc. (1994); among others.

Methods of the Invention

In one embodiment, the invention provides a method of inhibiting a function or decreasing stability of a Treg) comprising exposing said Treg to an inhibitor of Nrp1:semaphorin axis in said Treg. In one embodiment, such inhibitor of Nrp1:semaphorin axis inhibits interaction between a transmembrane semaphorin (e.g., class IV semaphorin such as, e.g., Sema4a) on conventional T cell and Nrp1 on the Treg. In one specific embodiment, the inhibitor of Nrp1:semaphorin axis does not affect Nrp1-VEGF interaction in said Treg. The inhibitor of Nrp1:semaphorin axis can be administered directly to a subject (e.g., human), e.g., a subject suffering from a cancer or an infection. In a related embodiment, the invention provides a method of treating a disease (e.g., a cancer or an infection) in a subject (e.g., human) in need thereof, the method comprising selectively inhibiting Nrp1:semaphorin axis in Tregs of the subject.

In one embodiment, the inhibitors of Nrp1:semaphorin axis useful in the methods of the invention are antibodies. In one specific embodiment, such antibodies do not affect Nrp1-VEGF interaction or Nrp1-semaphorin class III interaction in Tregs.

In another embodiment, the inhibitors of Nrp1:semaphorin axis useful in the methods of the invention are semaphorin molecules (e.g., a soluble version of sema4a protein or a fragment or a derivative or an analog thereof).

In yet another embodiment, the inhibitors of Nrp1:semaphorin axis useful in the methods of the invention are small molecules.

The present invention also encompasses inhibitors of Nrp1:semaphorin axis in Tregs which inhibit Nrp1 expression in Tregs, or locally (e.g., in tumors) inhibit transmembrane semaphorin expression on cells expressing such transmembrane semaphorin (e.g., conventional T cells (Tconv), conventional dendritic cells (cDCs), and/or plasmacytoid dendritic cells (pDCs)), or prevent Nrp1 from engaging with its downstream signaling pathway(s).

In a separate embodiment, the invention provides a method of enhancing a function or increasing stability of a Treg comprising exposing said Treg to an agonist of Nrp1:semaphorin axis in said Treg. In one embodiment, such agonist of Nrp1:semaphorin axis enhances interaction between a transmembrane semaphorin (e.g., class IV semaphorin such as, e.g., Sema4a) on conventional T cell and Nrp1 on the Treg. In one embodiment, the agonist of Nrp1:semaphorin axis is administered to the Treg in vitro (e.g., the Treg can be extracted from a subject (e.g., human suffering from an autoimmune or inflammatory disease), expanded ex vivo in the presence of an agonist of Nrp1-semaphorin interaction and then reintroduced back into the same subject or administered to a different subject). In another embodiment, the agonist of Nrp1:semaphorin axis can be administered directly to a subject (e.g., human), e.g., a subject suffering from an autoimmune or inflammatory disease. In a related embodiment, the invention provides a method of treating a disease (e.g., an autoimmune or inflammatory disease) in a subject (e.g., human) in need thereof, the method comprising selectively activating Nrp1:semaphorin axis in Tregs of the subject.

In one embodiment, the agonists of Nrp1:semaphorin axis useful in the methods of the invention are semaphorin molecules (e.g., Sema4a protein or a fragment or a derivative or an analog thereof). Such semaphorin molecules can be, e.g., multimerized and/or immobilized on a surface or a bead.

In another embodiment, the agonists of Nrp1:semaphorin axis useful in the methods of the invention are antibodies.

In yet another embodiment, the agonists of Nrp1:semaphorin axis useful in the methods of the invention are small molecules.

The present invention also encompasses the agonists of Nrp1:semaphorin axis in Tregs which enhance Nrp1 expression in Tregs, or locally (e.g., in pancreatic islets for diabetes) enhance semaphorin expression on cells expressing transmembrane semaphorin (e.g., conventional T cells (Tconv), conventional dendritic cells (cDCs), and/or plasmacytoid dendritic cells (pDCs)), or enhance Nrp1 engagement with its downstream signaling pathway(s).

Additional inhibitors and agonists of Nrp1:semaphorin axis on Treg can be identified using various screening methods known in the art (e.g., using immobilized target molecules or fragments thereof).

The inhibitors or agonists of the invention can be used in therapeutic methods described above or can be administered to a nonhuman mammal for the purposes of obtaining preclinical data. Exemplary nonhuman mammals to be treated include nonhuman primates, dogs, cats, rodents and other mammals in which preclinical studies are performed. Such mammals may be established animal models for a disease to be treated or may be used to study toxicity of the inhibitor or agonist of interest. In each of these embodiments, dose escalation studies may be performed in the mammal.

Non-limiting examples of cancers treatable by the methods of the invention include, for example, carcinomas, lymphomas, sarcomas, blastomas, and leukemias. Non-limiting specific examples, include, for example, breast cancer, pancreatic cancer, liver cancer, lung cancer, prostate cancer, colon cancer, renal cancer, bladder cancer, head and neck carcinoma, thyroid carcinoma, soft tissue sarcoma, ovarian cancer, primary or metastatic melanoma, squamous cell carcinoma, basal cell carcinoma, brain cancer, angiosarcoma, hemangiosarcoma, bone sarcoma, fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma, chordoma, angiosarcoma, endotheliosarcoma, lymphangiosarcoma, lymphangioendotheliosarcoma, synovioma, testicular cancer, uterine cancer, cervical cancer, gastrointestinal cancer, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, Waldenstroom's macroglobulinemia, papillary adenocarcinomas, cystadenocarcinoma, bronchogenic carcinoma, bile duct carcinoma, choriocarcinoma, seminoma, embryonal carcinoma, Wilms′ tumor, lung carcinoma, epithelial carcinoma, cervical cancer, testicular tumor, glioma, glioblastoma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, meningioma, retinoblastoma, leukemia, neuroblastoma, small cell lung carcinoma, bladder carcinoma, lymphoma, multiple myeloma, medullary carcinoma, B cell lymphoma, T cell lymphoma, myeloma, leukemia, chronic myeloid leukemia, acute myeloid leukemia, chronic lymphocytic leukemia, acute lymphocytic leukemia, hematopoietic neoplasias, thymoma, sarcoma, non-Hodgkins lymphoma, Hodgkins lymphoma, uterine cancer, renal cell carcinoma, hepatoma, etc.

The infections treatable by the methods of the present invention include, without limitation, any infections (in particular, chronic infections) in which Tregs are blocking sterilizing immunity and which can be caused by, for example, a bacterium, parasite, virus, fungus, or protozoa.

Non-limiting examples of the inflammatory and autoimmune diseases treatable by the methods of the present invention include, e.g., inflammatory bowel disease (IBD), ulcerative colitis, Crohn's disease, arthritis, diabetes, multiple sclerosis, such as, e.g., inflammatory bowel disease (IBD), ulcerative colitis, Crohn's disease, arthritis, diabetes mellitus type 1, multiple sclerosis, Graves' disease, lupus erythematosus, ankylosing spondylitis, psoriasis, Behcet's disease, autistic enterocolitis, Guillain-Barre Syndrome, myasthenia gravis, pemphigus vulgaris, acute disseminated encephalomyelitis (ADEM), transverse myelitis autoimmune cardiomyopathy, Celiac disease, dermatomyositis, Wegener's granulomatosis, allergy, asthma, contact dermatitis (including any reaction to a man-made chemical), atherosclerosis (or any other inflammatory condition affecting the heart or vascular system), etc.

It is contemplated that when used to treat various diseases, the inhibitors or agonists of the invention can be combined with other therapeutic agents suitable for the same or similar diseases. Also, two or more inhibitors or agonists of the invention may be also co-administered to generate additive or synergistic effects. When co-administered with a second therapeutic agent, the inhibitors or agonists of the invention and the second therapeutic agent may be simultaneously or sequentially (in any order). Suitable therapeutically effective dosages for each agent may be lowered due to the additive action or synergy.

The Nrp1:semaphorin axis agonists of the invention can be combined with other therapies that enhance Tregs (e.g., non-mitogenic anti-CD3), in vivo Treg transfer, or therapies that block inflammation (e.g., via blockage of ILL INFα/β, IL6, TNF, IL13, IL23, etc.).

In one embodiment, the inhibitors of Nrp1:semaphorin axis on Tregs disclosed herein are useful to enhance the efficacy of vaccines directed to infections or tumors. Similarly to vaccines against infections which contain inactivated cells of the infectious agent or a single or several antigens, tumor vaccines typically contain inactivated tumor cells or tumor antigens that stimulate a patient's immune system. The immune system responds to this stimulation by generating immunoresponsive cells that target the infection or neoplasia. As Tregs act to suppress such immune response, the inhibition of their function and stability by the methods of the invention can lead to enhanced immune response to vaccines.

The Treg inhibitors of the invention can be administered to a subject either simultaneously with or before (e.g., 1-14 days before) a reagent that acts to elicit an immune response (e.g., to treat cancer or an infection) is administered to the subject.

The inhibitory compounds of the invention can be also administered in combination with an anti-tumor antibody or an antibody directed at a pathogenic antigen.

The inhibitory treatments of the invention can be combined with other immunomodulatory treatments such as, e.g., therapeutic vaccines (including but not limited to GVAX, DC-based vaccines, etc.), checkpoint inhibitors (including but not limited to agents that block CTLA4, PD1, LAG3, TIM3, etc.) or activators (including but not limited to agents that enhance 41 BB, OX40, etc.). The inhibitory treatments of the invention can be also combined with other treatments that possess the ability to inhibit Treg function or stability. Some non-limiting examples of such additional Treg inhibitors include ONTAK, HuMax-Tac, Zenapax, and MDX-010.

Therapeutic methods of the invention can be combined with additional immunotherapies and therapies. For example, when used for treating cancer, inhibitors of the invention can be used in combination with conventional cancer therapies, such as, e.g., surgery, radiotherapy, chemotherapy or combinations thereof, depending on type of the tumor, patient condition, other health issues, and a variety of factors. In certain aspects, other therapeutic agents useful for combination cancer therapy with the inhibitors of the invention include anti-angiogenic agents. Many anti-angiogenic agents have been identified and are known in the art, including, e.g., TNP-470, platelet factor 4, thrombospondin-1, tissue inhibitors of metalloproteases (TIMP1 and TIMP2), prolactin (16-Kd fragment), angiostatin (38-Kd fragment of plasminogen), endostatin, bFGF soluble receptor, transforming growth factor beta, interferon alpha, soluble KDR and FLT-1 receptors, placental proliferin-related protein, as well as those listed by Carmeliet and Jain (2000). In one embodiment, the inhibitors of the invention can be used in combination with a VEGF antagonist or a VEGF receptor antagonist such as anti-VEGF antibodies, VEGF variants, soluble VEGF receptor fragments, aptamers capable of blocking VEGF or VEGFR, neutralizing anti-VEGFR antibodies, inhibitors of VEGFR tyrosine kinases and any combinations thereof (e.g., anti-hVEGF antibody A4.6.1, bevacizumab or ranibizumab).

Non-limiting examples of chemotherapeutic compounds which can be used in combination treatments of the present invention include, for example, aminoglutethimide, amsacrine, anastrozole, asparaginase, bcg, bicalutamide, bleomycin, buserelin, busulfan, campothecin, capecitabine, carboplatin, carmustine, chlorambucil, cisplatin, cladribine, clodronate, colchicine, cyclophosphamide, cyproterone, cytarabine, dacarbazine, dactinomycin, daunorubicin, dienestrol, diethylstilbestrol, docetaxel, doxorubicin, epirubicin, estradiol, estramnustine, etoposide, exemestane, filgrastim, fludarabine, fludrocortisone, fluorouracil, fluoxymesterone, flutamide, gemcitabine, genistein, goserelin, hydroxyurea, idarubicin, ifosfamide, imatinib, interferon, irinotecan, ironotecan, letrozole, leucovorin, leuprolide, levamisole, lomustine, mechlorethamine, medroxyprogesterone, megestrol, melphalan, mercaptopurine, mesna, methotrexate, mitomycin, mitotane, mitoxantrone, nilutamide, nocodazole, octreotide, oxaliplatin, paclitaxel, pamidronate, pentostatin, plicamycin, porfimer, procarbazine, raltitrexed, rituximab, streptozocin, suramin, tamoxifen, temozolomide, teniposide, testosterone, thioguanine, thiotepa, titanocene dichloride, topotecan, trastuzumab, tretinoin, vinblastine, vincristine, vindesine, and vinorelbine. These chemotherapeutic compounds may be categorized by their mechanism of action into, for example, following groups: anti-metabolites/anti-cancer agents, such as pyrimidine analogs (5-fluorouracil, floxuridine, capecitabine, gemcitabine and cytarabine) and purine analogs, folate antagonists and related inhibitors (mercaptopurine, thioguanine, pentostatin and 2-chlorodeoxyadenosine (cladribine)); antiproliferative/antimitotic agents including natural products such as vinca alkaloids (vinblastine, vincristine, and vinorelbine), microtubule disruptors such as taxane (paclitaxel, docetaxel), vincristin, vinblastin, nocodazole, epothilones and navelbine, epidipodophyllotoxins (etoposide, teniposide), DNA damaging agents (actinomycin, amsacrine, anthracyclines, bleomycin, busulfan, camptothecin, carboplatin, chlorambucil, cisplatin, cyclophosphamide, cytoxan, dactinomycin, daunorubicin, doxorubicin, epirubicin, hex amethyhnelamineoxaliplatin, iphosphamide, melphalan, merchlorehtamine, mitomycin, mitoxantrone, nitrosourea, plicamycin, procarbazine, taxol, taxotere, teniposide, triethylenethiophosphoramide and etoposide (VP16)); antibiotics such as dactinomycin (actinomycin D), daunorubicin, doxorubicin (adriamycin), idarubicin, anthracyclines, mitoxantrone, bleomycins, plicamycin (mithramycin) and mitomycin; enzymes (L-asparaginase which systemically metabolizes L-asparagine and deprives cells which do not have the capacity to synthesize their own asparagine); antiplatelet agents; antiproliferative/antimitotic alkylating agents such as nitrogen mustards (mechlorethamine, cyclophosphamide and analogs, melphalan, chlorambucil), ethylenimines and methylmelamines (hexamethylmelamine and thiotepa), alkyl sulfonates-busulfan, nitrosoureas (carmustine (BCNU) and analogs, streptozocin), trazenes-dacarbazinine (DTIC); antiproliferative/antimitotic antimetabolites such as folic acid analogs (methotrexate); platinum coordination complexes (cisplatin, carboplatin), procarbazine, hydroxyurea, mitotane, aminoglutethimide; hormones, hormone analogs (estrogen, tamoxifen, goserelin, bicalutamide, nilutamide) and aromatase inhibitors (letrozole, anastrozole); anticoagulants (heparin, synthetic heparin salts and other inhibitors of thrombin); fibrinolytic agents (such as tissue plasminogen activator, streptokinase and urokinase), aspirin, dipyridamole, ticlopidine, clopidogrel, abciximab; antimigratory agents; antisecretory agents (breveldin); immunosuppressives (cyclosporine, tacrolimus (FK-506), sirolimus (rapamycin), azathioprine, mycophenolate mofetil); anti-angiogenic compounds (e.g., TNP-470, genistein, bevacizumab) and growth factor inhibitors (e.g., fibroblast growth factor (FGF) inhibitors); angiotensin receptor blocker; nitric oxide donors; anti-sense oligonucleotides; antibodies (trastuzumab); cell cycle inhibitors and differentiation inducers (tretinoin); mTOR inhibitors, topoisomerase inhibitors (doxorubicin (adriamycin), amsacrine, camptothecin, daunorubicin, dactinomycin, eniposide, epirubicin, etoposide, idarubicin and mitoxantrone, topotecan, irinotecan), corticosteroids (cortisone, dexamethasone, hydrocortisone, methylpednisolone, prednisone, and prenisolone); growth factor signal transduction kinase inhibitors; mitochondrial dysfunction inducers and caspase activators; and chromatin disruptors.

For treatment of infections, combined therapy of the invention can encompass co-administering Treg inhibitors of the invention with an antibiotic, an anti-fungal drug, an anti-viral drug, an anti-parasitic drug, an anti-protozoal drug, or a combination thereof.

Non-limiting examples of useful antibiotics include lincosamides (clindomycin); chloramphenicols; tetracyclines (such as Tetracycline, Chlortetracycline, Demeclocycline, Methacycline, Doxycycline, Minocycline); aminoglycosides (such as Gentamicin, Tobramycin, Netilmicin, Amikacin, Kanamycin, Streptomycin, Neomycin); beta-lactams (such as penicillins, cephalosporins, Imipenem, Aztreonam); vancomycins; bacitracins; macrolides (erythromycins), amphotericins; sulfonamides (such as Sulfanilamide, Sulfamethoxazole, Sulfacetamide, Sulfadiazine, Sulfisoxazole, Sulfacytine, Sulfadoxine, Mafenide, p-Aminobenzoic Acid, Trimethoprim-Sulfamethoxazole); Methenamin; Nitrofurantoin; Phenazopyridine; trimethoprim; rifampicins; metronidazoles; cefazolins; Lincomycin; Spectinomycin; mupirocins; quinolones (such as Nalidixic Acid, Cinoxacin, Norfloxacin, Ciprofloxacin, Pefloxacin, Ofloxacin, Enoxacin, Fleroxacin, Levofloxacin); novobiocins; polymixins; gramicidins; and antipseudomonals (such as Carbenicillin, Carbenicillin Indanyl, Ticarcillin, Azlocillin, Mezlocillin, Piperacillin) or any salts or variants thereof. See also Physician's Desk Reference, 59.sup.th edition, (2005), Thomson P D R, Montvale N.J.; Gennaro et al., Eds. Remington's The Science and Practice of Pharmacy, 20.sup.th edition, (2000), Lippincott Williams and Wilkins, Baltimore Md.; Braunwald et al., Eds. Harrison's Principles of Internal Medicine, 15.sup.th edition, (2001), McGraw Hill, NY; Berkow et al., Eds. The Merck Manual of Diagnosis and Therapy, (1992), Merck Research Laboratories, Rahway N.J. Such antibiotics can be obtained commercially, e.g., from Daiichi Sankyo, Inc. (Parsipanny, N.J.), Merck (Whitehouse Station, N.J.), Pfizer (New York, N.Y.), Glaxo Smith Kline (Research Triangle Park, N.C.), Johnson & Johnson (New Brunswick, N.J.), AstraZeneca (Wilmington, Del.), Novartis (East Hanover, N.J.), and Sanofi-Aventis (Bridgewater, N.J.). The antibiotic used will depend on the type of bacterial infection.

Non-limiting examples of useful anti-fungal agents include imidazoles (such as griseofulvin, miconazole, terbinafine, fluconazole, ketoconazole, voriconazole, and itraconizole); polyenes (such as amphotericin B and nystatin); Flucytosines; and candicidin or any salts or variants thereof. See also Physician's Desk Reference, 59.sup.th edition, (2005), Thomson P D R, Montvale N.J.; Gennaro et al., Eds. Remington's The Science and Practice of Pharmacy 20.sup.th edition, (2000), Lippincott Williams and Wilkins, Baltimore Md.; Braunwald et al., Eds. Harrison's Principles of Internal Medicine, 15.sup.th edition, (2001), McGraw Hill, NY; Berkow et al., Eds. The Merck Manual of Diagnosis and Therapy, (1992), Merck Research Laboratories, Rahway N.J.

Non-limiting examples of useful anti-viral drugs include interferon alpha, beta or gamma, didanosine, lamivudine, zanamavir, lopanivir, nelfinavir, efavirenz, indinavir, valacyclovir, zidovudine, amantadine, rimantidine, ribavirin, ganciclovir, foscarnet, and acyclovir or any salts or variants thereof. See also Physician's Desk Reference, 59.sup.th edition, (2005), Thomson P D R, Montvale N.J.; Gennaro et al., Eds. Remington's The Science and Practice of Pharmacy 20.sup.th edition, (2000), Lippincott Williams and Wilkins, Baltimore Md.; Braunwald et al., Eds. Harrison's Principles of Internal Medicine, 15.sup.th edition, (2001), McGraw Hill, NY; Berkow et al., Eds. The Merck Manual of Diagnosis and Therapy, (1992), Merck Research Laboratories, Rahway N.J.

Non-limiting examples of useful anti-parasitic agents include chloroquine, mefloquine, quinine, primaquine, atovaquone, sulfasoxine, and pyrimethamine or any salts or variants thereof. See also Physician's Desk Reference, 59.sup.th edition, (2005), Thomson P D R, Montvale N.J.; Gennaro et al., Eds. Remington's The Science and Practice of Pharmacy 20.sup.th edition, (2000), Lippincott Williams and Wilkins, Baltimore Md.; Braunwald et al., Eds. Harrison's Principles of Internal Medicine, 15.sup.th edition, (2001), McGraw Hill, NY; Berkow et al., Eds. The Merck Manual of Diagnosis and Therapy, (1992), Merck Research Laboratories, Rahway N.J.

Non-limiting examples of useful anti-protozoal drugs include metronidazole, diloxanide, iodoquinol, trimethoprim, sufamethoxazole, pentamidine, clindamycin, primaquine, pyrimethamine, and sulfadiazine or any salts or variants thereof. See also Physician's Desk Reference, 59.sup.th edition, (2005), Thomson P D R, Montvale N.J.; Gennaro et al., Eds. Remington's The Science and Practice of Pharmacy 20.sup.th edition, (2000), Lippincott Williams and Wilkins, Baltimore Md.; Braunwald et al., Eds. Harrison's Principles of Internal Medicine, 15.sup.th edition, (2001), McGraw Hill, NY; Berkow et al., Eds. The Merck Manual of Diagnosis and Therapy, (1992), Merck Research Laboratories, Rahway N.J.

Antibody Inhibitors and Agonists of the Invention

In conjunction with the above methods, the invention provides isolated antibodies which inhibit or augment Nrp1:semaphorin interaction on Tregs. In one embodiment, the semaphorin is class IV semaphorin (e.g., Sema4a). In one embodiment, the antibodies do not affect Nrp1-VEGF interaction or Nrp1-semaphorin class III interaction in Tregs.

The invention encompasses both anti-Nrp1 and anti-semaphorin antibodies which interfere with Nrp-1:semaphorin interaction on Tregs. Examples of useful antibodies include, for example, (i) antibodies which specifically target “sema” and “PSI” domains of semaphorin molecules, an evolutionarily conserved region on all semaphorin molecules (see, e.g., Takamatsu and Kumanogoh, Trends Immunol., 2012, 33(3):127-135) as well as (ii) antibodies which target the semaphorin-binding domain on Nrp1 (rather than the VEGF-binding domain) (see, e.g., Parker et al., J. Biol. Chem., 2012, 287(14):11082-11089).

For both inhibitory and potentiating antibodies, the invention also provides bispecific antibodies which, in addition to Nrp1, also recognize a Treg-specific protein and therefore target the antibody specifically to Tregs. For example, such bispecific antibodies, in addition to Nrp1, can target a surface protein of the Tregs, which include, for example, CD25, CD4, CD28, CD38, CD62L (selectin), OX-40 ligand (OX-404 CTLA4, CCR4, CCR8, FOXP3, LAG3, CD103, glucocorticoid-induced TNF receptor (GITR), galectin-1, TNFR2, or TGFβR1.

The antibodies for use in accordance with the present invention may be monoclonal or polyclonal as appropriate. The antibody fragments can be also used and include, for example, Fab, Fab′, F(ab)₂ or Fv fragments. The antibody may be a single chain antibody. Other suitable modifications and/or agents will be apparent to those skilled in the art. Chimeric and humanized antibodies are also within the scope of the invention. It is expected that chimeric and humanized antibodies would be less immunogenic in a human subject than the corresponding non-chimeric antibody. A variety of approaches for making chimeric antibodies, comprising for example a non-human variable region and a human constant region, have been described. See, for example, Morrison et al., Proc. Natl. Acad. Sci. U.S.A. 81, 6851 (1985); Takeda, et al., Nature 314, 452 (1985), Cabilly et al., U.S. Pat. No. 4,816,567; Boss et al., U.S. Pat. No. 4,816,397; Tanaguchi et al., European Patent Publication EP 171496; European Patent Publication 0173494, United Kingdom Patent GB 2177096B. Additionally, a chimeric antibody can be further “humanized” such that parts of the variable regions, especially the conserved framework regions of the antigen-binding domain, are of human origin and only the hypervariable regions are of non-human origin. Such altered immunoglobulin molecules may be made by any of several techniques known in the art, (e.g., Teng et al., Proc. Natl. Acad. Sci. U.S.A., 80, 7308-7312 (1983); Kozbor et al., Immunology Today, 4, 7279 (1983); Olsson et al., Meth. Enzymol., 92, 3-16 (1982)), and are preferably made according to the teachings of PCT Publication WO92/06193 or EP 0239400. Humanized antibodies can be commercially produced by, for example, Scotgen Limited, 2 Holly Road, Twickenham, Middlesex, Great Britain.

In certain embodiments, anti-idiotypic antibodies are also provided. Anti-idiotypic antibodies recognize antigenic determinants associated with the antigen-binding site of another antibody. Anti-idiotypic antibodies can be prepared against a second antibody by immunizing an animal of the same species, and preferably of the same strain, as the animal used to produce the second antibody. See, e.g., U.S. Pat. No. 4,699,880. In one embodiment, antibodies are raised against Nrp1 or semaphorin or a portion thereof, and these antibodies are used in turn to produce an anti-idiotypic antibody.

The present invention provides antibodies for both intracellular and extracellular targeting. Intracellular targeting can be accomplished through the use of intracellularly expressed antibodies referred to as intrabodies.

To screen for additional antibodies which bind to a particular epitope on the antigen of interest (e.g., Nrp1 or Sema4a), a routine cross-blocking assay such as that described in Antibodies, A Laboratory Manual, Cold Spring Harbor Laboratory, Ed Harlow and David Lane (1988), can be performed. Alternatively, epitope mapping, e.g. as described in Champe et al. (1995) J. Biol. Chem. 270:1388-1394, can be performed to determine whether the antibody binds an epitope of interest.

Additional antibodies useful in the present invention can be also generated and selected using phage display approach as described, e.g. in U.S. Patent Appl. Publ. No. 2008/0213268.

Antibodies of the invention can be further modified to generate antibody mutants with improved physical, chemical and or biological properties over the parent antibody. Where the assay used is a biological activity assay, the antibody mutant preferably has a biological activity in the assay of choice (e.g., measuring a function or stability of a Treg via Transwell suppression assay and upregulation of Bcl2 or Helios) which is at least about 10 fold better, preferably at least about 20 fold better, more preferably at least about 50 fold better, and sometimes at least about 100 fold or 200 fold better, than the biological activity of the parent antibody in that assay.

To generate the antibody mutant, one or more amino acid alterations (e.g. substitutions) can be introduced in one or more of the hypervariable regions of the parent antibody. Alternatively, or in addition, one or more alterations (e.g., substitutions) of framework region residues may be introduced in the parent antibody where these result in an improvement in the binding affinity of the antibody mutant for the antigen from the second mammalian species. Examples of framework region residues to modify include those which non-covalently bind antigen directly (Amit et al. (1986) Science 233:747-753); interact with/effect the conformation of a CDR (Chothia et al. (1987) J. Mol. Biol. 196:901-917); and/or participate in the V_(L)-V_(H) interface (EP 239400B1). In certain embodiments, modification of one or more of such framework region residues results in an enhancement of the binding affinity of the antibody for the antigen from the second mammalian species. For example, from about one to about five framework residues may be altered in this embodiment of the invention. Sometimes, this may be sufficient to yield an antibody mutant suitable for use in preclinical trials, even where none of the hypervariable region residues have been altered. Normally, however, the antibody mutant will comprise additional hypervariable region alteration(s). The hypervariable region residues which are altered may be changed randomly, especially where the starting binding affinity of the parent antibody is such that such randomly produced antibody mutants can be readily screened.

One useful procedure for generating such antibody mutants is called “alanine scanning mutagenesis” (Cunningham and Wells (1989) Science 244:1081-1085). Here, one or more of the hypervariable region residue(s) are replaced by alanine or polyalanine residue(s) to affect the interaction of the amino acids with the antigen from the second mammalian species. Those hypervariable region residue(s) demonstrating functional sensitivity to the substitutions then are refined by introducing further or other mutations at or for the sites of substitution. The ala-mutants produced this way are screened for their biological activity as described herein.

Antibodies of the invention can be prepared by standard means.

For preparation of immunizing antigen, and polyclonal and monoclonal antibody production see, e.g., Kohler et al., Nature 256:495-497 (1975) and Eur. J. Immunol. 6:511-519 (1976); Milstein et al., Nature 266:550-552 (1977); Koprowski et al., U.S. Pat. No. 4,172,124; Harlow and Lane, “Antibodies: A Laboratory Manual,” (Cold Spring Harbor Laboratory: Cold Spring Harbor, N.Y., 1988); and “Current Protocols In Molecular Biology,” (Ausubel et al., Eds.; John Wiley & Sons: New York, N.Y., 1991); Kozbar et al., Immunology Today 4:72 (1983)), Cole et al., “Monoclonal Antibodies and Cancer Therapy” (Alan R. Liss, Inc. pp. 77-96 (1985)). Cells which produce antibodies with the desired specificity can be selected by a suitable assay (e.g., ELISA).

The antibodies of the invention can be also produced recombinantly, using well-known techniques. See, e.g., Cabilly et al., U.S. Pat. No. 4,816,567; Winter, U.S. Pat. No. 5,225,539. A nucleic acid encoding a desired antigen can be isolated or synthethized using conventional procedures and inserted into a replicable vector for further cloning or for expression.

When using recombinant techniques, the antibody can be produced intracellularly, in the periplasmic space, or directly secreted into the medium and further isolated and purified using known techniques such as, for example, hydroxylapatite chromatography, gel electrophoresis, dialysis, and affinity chromatography. Protein A affinity chromatography can be used to purify antibodies that are based on human γ1, γ2, or γ4 heavy chains (Lindmark et al. (1983) J. Immunol. Meth. 62:1-13). Protein G affinity chromatography can be used for mouse isotypes and for human γ3 (Guss et al. (1986) EMBO J. 5:15671575).

The various portions of chimeric, humanized, primatized (CDR-grafted) antibodies, or CDR-grafted single chain antibodies, comprising portions derived from different species, antibodies can be joined together chemically by conventional techniques, or can be prepared as a contiguous protein using genetic engineering techniques. For example, nucleic acids encoding a chimeric or humanized chain can be expressed to produce a contiguous protein. See, e.g., Cabilly et al., U.S. Pat. No. 4,816,567; Cabilly et al., European Patent No. 0,125,023 B1; Boss et al., U.S. Pat. No. 4,816,397; Boss et al., European Patent No. 0,120,694 B1; Neuberger et al., WO 86/01533; Neuberger et al., European Patent No. 0,194,276 B1; Winter, U.S. Pat. No. 5,225,539; and Winter, European Patent No. 0,239,400 B1. See also, Newman et al., BioTechnology 10:1455-1460 (1992), regarding primatized antibody and Ladner et al., U.S. Pat. No. 4,946,778 and Bird et al., Science 242:423-426 (1988)), regarding single chain antibodies. Nucleic acid (e.g., DNA) sequences coding for humanized variable regions can be constructed using PCR mutagenesis methods to alter DNA sequences encoding a human or humanized chain, such as a DNA template from a previously humanized variable region (see, e.g., Kamman et al., Nucl. Acids Res., 17:5404 (1989)); Sato et al., Cancer Research 53:851-856 (1993); Daugherty et al., Nucleic Acids Res. 19(9):2471-2476 (1991); and Lewis and Crowe, Gene 101:297-302 (1991)). Using these or other suitable methods, variants can also be readily produced. In one embodiment, cloned variable regions can be mutagenized, and sequences encoding variants with the desired specificity can be selected (e.g., from a phage library; see, e.g., Krebber et al., U.S. Pat. No. 5,514,548; and Hoogenboom et al., WO 93/06213).

In addition, functional fragments of antibodies, including fragments of chimeric, humanized, primatized, or single chain antibodies can also be produced. Functional fragments of the subject antibodies retain at least one binding function and/or modulation function of the full-length antibody from which they are derived. Useful antibody fragments include, but are not limited to, Fv, Fab, Fab′ and F(ab′)₂ fragments. Such fragments can be produced by enzymatic cleavage or by recombinant techniques. For instance, papain or pepsin cleavage can generate Fab or F(ab′)₂ fragments, respectively. Antibodies can also be produced in a variety of truncated forms using antibody genes in which one or more stop codons has been introduced upstream of the natural stop site. For example, a chimeric gene encoding a F(ab′)₂ heavy chain portion can be designed to include DNA sequences encoding the CH1 domain and hinge region of the heavy chain.

Other suitable methods of producing or isolating antibodies of the requisite specificity can be used, including, for example, methods which select recombinant antibody from a library, or which rely upon immunization of transgenic animals (e.g., mice) capable of producing a full repertoire of human antibodies. See, e.g., Jakobovits et al., Proc. Natl. Acad. Sci. USA 90:2551-2555 (1993); Jakobovits et al., Nature 362:255-258 (1993); Lonberg et al., U.S. Pat. No. 5,545,806; Surani et al., U.S. Pat. No. 5,545,807; Cabilly et al., U.S. Pat. No. 4,816,567; Cabilly et al., European Patent No. 0,125,023 B1; Queen et al., European Patent No. 0,451,216 B1; Boss et al., U.S. Pat. No. 4,816,397; Boss et al., European Patent No. 0,120,694 E1; Neuberger et al., WO 86/01533; Neuberger et al., European Patent No. 0,194,276 B1; Winter, U.S. Pat. No. 5,225,539; Winter, European Patent No. 0,239,400 B1; and Padlan et al., European Patent Application No. 0,519,596 A1. See, also, Ladner et al., U.S. Pat. No. 4,946,778; Huston, U.S. Pat. No. 5,476,786; and Bird et al., Science 242: 423-426 (1988).

In certain embodiments, the antibodies or antigen binding fragments of the antibodies can be labeled or unlabeled and used for diagnostic purposes. Typically, diagnostic assays entail detecting the formation of a complex resulting from the binding of an antibody to its target. The antibodies can be directly labeled with, for example, a radionuclide, a fluorophore, an enzyme, an enzyme substrate, an enzyme cofactor, an enzyme inhibitor, and a ligand (e.g., biotin or a hapten). Numerous appropriate immunoassays are known to the skilled artisan (see, e.g., U.S. Pat. Nos. 3,817,827; 3,850,752; 3,901,654; and 4,098,876).

Pharmaceutical compositions comprising the antibodies of the invention can be prepared by mixing the antibody having the desired degree of purity with optional physiologically acceptable carriers, excipients or stabilizers (Remington's Pharmaceutical Sciences 16th edition, Osol, A. Ed. (1980)), in the form of lyophilized formulations or aqueous solutions. Acceptable carriers, excipients, or stabilizers are nontoxic to recipients at the dosages and concentrations employed, and include buffers such as phosphate, citrate, and other organic acids; antioxidants including ascorbic acid and methionine; preservatives (such as octadecyldimethylbenzyl ammonium chloride; hexamethonium chloride; benzalkonium chloride, benzethonium chloride; phenol, butyl or benzyl alcohol; alkyl parabens such as methyl or propyl paraben; catechol; resorcinol; cyclohexanol; 3-pentanol; and m-cresol); low molecular weight (less than about 10 residues) polypeptide; proteins, such as serum albumin, gelatin, or immunoglobulins; hydrophilic polymers such as polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagine, histidine, arginine, or lysine; monosaccharides, disaccharides, and other carbohydrates including glucose, mannose, or dextrins; chelating agents such as EDTA; sugars such as sucrose, mannitol, trehalose or sorbitol; salt-forming counter-ions such as sodium; metal complexes (e.g., Zn-protein complexes); and/or non-ionic surfactants such as TWEEN™, PLURONICS™ or polyethylene glycol (PEG).

The pharmaceutical compositions comprising the antibodies of the invention may also contain one or more additional active compounds as necessary for the particular indication being treated, preferably those with complementary activities that do not adversely affect each other. Various active agents can be present in combination in amounts that are effective for the purpose intended. Non-limiting examples of possible additional active compounds include, e.g., IL2 and TGFβ as well as various agents listed in the discussion of combination treatments, above.

The active ingredients may be entrapped in microcapsule prepared, for example, by coacervation techniques or by interfacial polymerization, for example, hydroxymethylcellulose or gelatin-microcapsule and poly-(methylmethacylate) microcapsule, respectively, in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules) or in macroemulsions. Such techniques are disclosed in Remington's Pharmaceutical Sciences 16th edition, Osol, A. Ed. (1980).

Sustained-release preparations may be also prepared. Suitable examples of sustained-release preparations include semipermeable matrices of solid hydrophobic polymers containing the antibody, which matrices are in the form of shaped articles, e.g., films, or microcapsule. Examples of sustained-release matrices include polyesters, hydrogels (for example, poly(2-hydroxyethyl-methacrylate), or poly(vinylalcohol)), polylactides (U.S. Pat. No. 3,773,919), copolymers of L-glutamic acid and .gamma. ethyl-L-glutamate, non-degradable ethylene-vinyl acetate, degradable lactic acid-glycolic acid copolymers such as the LUPRON DEPOT™ (injectable microspheres composed of lactic acid-glycolic acid copolymer and leuprolide acetate), and poly-D-(−)-3-hydroxybutyric acid. While polymers such as ethylene-vinyl acetate and lactic acid-glycolic acid enable release of molecules for over 100 days, certain hydrogels release proteins for shorter time periods. When encapsulated antibodies remain in the body for a long time, they may denature or aggregate as a result of exposure to moisture at 37° C., resulting in a loss of biological activity and possible changes in immunogenicity. Rational strategies can be devised for stabilization depending on the mechanism involved. For example, if the aggregation mechanism is discovered to be intermolecular S-S bond formation through thio-disulfide interchange, stabilization may be achieved by modifying sulfhydryl residues, lyophilizing from acidic solutions, controlling moisture content, using appropriate additives, and developing specific polymer matrix compositions.

For the treatment of a disease, the appropriate dosage of antibody of the invention will depend on the type of disease to be treated, the severity and course of the disease, whether the antibody is administered for preventive or therapeutic purposes, previous therapy, the patient's clinical history and response to the antibody, and the discretion of the attending physician. The antibody can be administered to the patient at one time or over a series of treatments. The progress of the therapy of the invention can be easily monitored by conventional techniques and assays.

The administration of antibodies of the invention can be performed by any suitable route, including systemic administration as well as administration directly to the site of the disease (e.g., to primary tumor or chronic infection site).

Protein/Peptide Inhibitors and Agonists of the Invention

As specified above, the inhibitors of Nrp1:semaphorin axis useful in the methods of the invention include various semaphorin molecules, such as, for example, soluble versions of transmembrane semaphorin proteins (e.g., Sema4a) as well as various inhibitory fragments, derivatives, and analogs thereof. Also included within the present invention are soluble extracellular domains of Nrp1 which can function as competitive inhibitors of Nrp1:semaphorin axis as well as various inhibitory fragments, derivatives, and analogs thereof. In one specific embodiment, the inhibitory semaphorin molecule is Sema4a-Ig fusion protein, which is a fusion (at the C-terminus) between Sema4a extracellular domain (Met1-His683 fragment of GenBank Accession No. NP_(—)038686) and the Fc region of human or murine IgG1. In one specific embodiment, the inhibitory semaphorin molecule is a fragment of Nrp1 protein (or a derivative or an analog thereof) comprising all or part of Nrp1 cytoplasmic domain comprising the C-terminal amino acid sequence SEA, which molecule inhibits a signaling pathway between the cytoplasmic domain of Nrp1 protein and PTEN protein.

As further discussed above, the agonists of Nrp1:semaphorin axis useful in the methods of the invention also include various semaphorin molecules, including full-length semaphorin proteins (e.g., Sema4a protein) as well as agonist fragments, derivatives, and analogs thereof. Such agonist semaphorin molecules can be, e.g., multimerized (e.g., using IgM fusion proteins) and/or immobilized on a surface or a bead.

Soluble inhibitory versions of transmemebrane semaphorin proteins include, for example, their complete extracellular domains (e.g., the entire extracellular domain of Sema4a) or Nrp1-binding portions of such extracellular domains (e.g., fused to an Fc domain) which are capable of binding with high affinity and specificity to Nrp1 without potentiating Nrp1:semaphorin axis on Tregs. In some embodiments, such inhibitory versions of transmembrane semaphorin proteins do not affect Nrp1-VEGF interaction in Tregs. Soluble inhibitory versions of extracellular domains of Nrp1 include, for example, the entire extracellular domain of Nrp1 or Sema4a-binding portions of such extracellular domain (e.g., fused to an Fc domain) which are capable of binding with high affinity and specificity to Sema4a without potentiating Nrp1:semaphorin axis on Tregs. The effectiveness of semaphorin molecules or fragments or soluble inhibitory versions of extracellular domains of Nrp1 to inhibit Nrp1:semaphorin axis on Tregs can be tested using assays known in the art and those outlined in the Examples section, specifically the Transwell suppression assay.

Semaphorin proteins and fragments can be produced recombinantly from the corresponding fragments of the nucleic acids using various expression systems well known in the art and a variety of host systems are suitable for production, including bacteria (e.g., E. coli), yeast (e.g., Saccharomyces cerevisiae), insect (e.g., Sf9), and mammalian cells (e.g., CHO, COS-7). Many expression vectors have been developed and are available for each of these hosts. Vectors and procedures for cloning and expression are discussed, for example, in Sambrook et al. (Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1987)) and in Ausubel et al., 1995. Standard expression vectors useful in the current invention are well known in the art and include (but are not limited to) plasmids, cosmids, phage vectors, viral vectors, and yeast artificial chromosomes. The vector sequences may contain a replication origin for propagation in Escherichia coli (E. coli); the SV40 origin of replication; an ampicillin, neomycin, or puromycin resistance gene for selection in host cells; and/or genes (e.g., dihydrofolate reductase gene) that amplify the dominant selectable marker plus the gene of interest.

In some embodiments, the DNA sequence is cloned into a vector to create a fusion protein. The fusion partner may function to allow the fusion protein to be visualized or detected. For example, the fusion partner may contain an epitope that is recognized by an antibody, a domain that binds to a peptide or nucleic acid, or a peptide that is more readily detectable. Fusion partner include, but are not limited to, HA, myc, His₆, Green Fluorescent Protein (GFP), glutathione-S-transferase (GST), protein A from Staphylococcus aureus, two synthetic IgG-binding domains (ZZ) of protein A, outer membrane protein F, β-galactosidase (lacZ), and various products of bacteriophage λ and bacteriophage T7. From the teachings provided herein, it is apparent that other proteins may be used as fusion partners. To facilitate isolation of the GNAL sequence from the fusion protein, amino acids susceptible to chemical cleavage (e.g., CNBr) or enzymatic cleavage (e.g., V8 protease, trypsin) may be used to bridge the GNAL protein and the fusion partner.

Preferably, the expression vector of the invention contains a promoter sequence. Suitable promoters, including both constitutive and inducible promoters, are widely available and are well known in the art. Commonly used promoters for expression in bacteria include promoters from T7, T3, T5, and SP6 phages, and the tip, lpp, and lac operons. Hybrid promoters (see, U.S. Pat. No. 4,551,433), such as tac and trc, may also be used. Examples of plasmids for expression in bacteria include the pET expression vectors pET3a, pET 11a, pET 12a-c, and pET 15b (see U.S. Pat. No. 4,952,496; available from Novagen, Madison, Wis.). Low copy number vectors (e.g., pPD100) can be used for efficient overproduction of peptides deleterious to the E. coli host (Dersch et al., FEMS Microbiol. Lett. 123: 19, 1994). Bacterial hosts for the T7 expression vectors may contain chromosomal copies of DNA encoding T7 RNA polymerase operably linked to an inducible promoter (e.g., lacUV promoter; see, U.S. Pat. No. 4,952,496), such as found in the E. coli strains HMS174(DE3)pLysS, BL21(DE3)pLysS, HMS174(DE3) and BL21(DE3). T7 RNA polymerase can also be present on plasmids compatible with the T7 expression vector. The polymerase may be under control of a lambda promoter and repressor (e.g., pGP1-2; Tabor and Richardson, Proc. Natl. Acad. Sci. USA (1985) 82: 1074, 1985).

Other promoters that may be used to control expression include, but are not limited to, cytomegalovirus (CMV) promoter (U.S. Pat. Nos. 5,385,839 and 5,168,062), the SV40 early promoter region (Benoist and Chambon, Nature 1981, 290:304-310), the promoter contained in the 3′ long terminal repeat of Rous sarcoma virus (Yamamoto, et al., Cell 1980, 22:787-797), the herpes thymidine kinase promoter (Wagner et al., Proc. Natl. Acad. Sci. U.S.A. (1981) 78: 1441-1445), the regulatory sequences of the metallothionein gene (Brinster et al., Nature 1982; 296:39 42); prokaryotic expression vectors such as the β-lactamase promoter (Villa-Komaroff et al., Proc. Natl. Acad. Sci. U.S.A. (1978) 75: 3727-3731), or the tac promoter (DeBoer et al., Proc. Natl. Acad. Sci. U.S.A. 1983; 80:21-25); see also “Useful proteins from recombinant bacteria” in Scientific American 1980; 242:74-94. Still other useful promoters that may be used include promoter elements from yeast or other fungi such as the Gal4 promoter, the ADC (alcohol dehydrogenase) promoter, PGK (phosphoglycerol kinase) promoter, alkaline phosphatase promoter; and transcriptional control regions that exhibit hematopoietic tissue specificity, in particular: beta-globin gene control region which is active in myeloid cells (Mogram et al., Nature 1985; 315:338-340; Kollias et al., Cell 1986; 46:89-94), hematopoietic stem cell differentiation factor promoters, erythropoietin receptor promoter (Maouche et al., Blood 1991; 15:2557), etc.

Other regulatory sequences may also be included in expression vectors of the invention. Such sequences include an enhancer, ribosome binding site, transcription termination signal sequence, secretion signal sequence, origin of replication, selectable marker, and the like. The regulatory sequences are operably linked with one another to allow transcription and subsequent translation.

The presence of a particular codon may have an adverse effect on expression in a particular host; therefore, a nucleic acid sequence may be optimized for a particular host system, such as prokaryotic or eukaryotic cells. Methods for altering nucleotide sequences to alleviate the codon usage problem are well known to those of skill in the art (see, e.g., Kane, Curr. Opin. Biotechnol. (1995) 6: 494; Makrides, Microbiol. Rev. (1996) 60: 512; and Brown (Ed.), Molecular Biology LabFax, BIOS Scientific Publishers, Ltd. (1991), which provides a Codon Usage Table at page 245 through page 253).

Soluble forms of the protein can be obtained by collecting culture fluid, or solubilizing-inclusion bodies, e.g., by treatment with detergent, and if desired sonication or other mechanical processes, as described above. The solubilized or soluble protein can be isolated using various techniques, such as polyacrylamide gel electrophoresis (PAGE), isoelectric focusing, 2 dimensional gel electrophoresis, chromatography (e.g., ion exchange, affinity, immunoaffinity, and sizing column chromatography), centrifugation, differential solubility, immunoprecipitation, or by any other standard technique for the purification of proteins.

Alternatively, semaphorin proteins or fragments of the invention can be chemically synthesized using techniques known in the art such as, e.g., conventional Merrifield solid phase f-Moc or t-Boc chemistry. For methods of peptide synthesis see also Bodansky, “Principles of Peptide Synthesis,” (Springer Verlag, Berlin (1993)) and Grant (ed.), “Synthetic Peptides: A User's Guide,” (W. H. Freeman and Company, New York (1992)). In addition, automated peptide synthesizers are commercially available (e.g., Advanced ChemTech Model 396; Milligen/Biosearch 9600).

In certain embodiments, the present invention contemplates making functional variants of semaphorin molecules by modifying their structure in order to enhance therapeutic efficacy or stability (e.g., ex vivo shelf life and resistance to proteolytic degradation in vivo). Modified polypeptides can be produced, for instance, by amino acid substitution, deletion, or addition. For example, it is reasonable to expect that an isolated replacement of a leucine with an isoleucine or valine, an aspartate with a glutamate, a threonine with a serine, or a similar replacement of an amino acid with a structurally related amino acid (e.g., conservative mutations) will not have a major effect on the biological activity of the resulting molecule. Conservative replacements are those that take place within a family of amino acids that are related in their side chains. For additional methods, see, e.g., Levin et al., Nature, 2012, 484(7395):529-533.

The present disclosure further contemplates a method of generating sets of combinatorial mutants of the semaphorin polypeptides, as well as truncation mutants and functional variant sequences by screening combinatorial libraries. There are many ways by which a library of potential homologs can be generated from a degenerate oligonucleotide sequence. Chemical synthesis of a degenerate gene sequence can be carried out in an automatic DNA synthesizer, and the synthetic genes can then be ligated into an appropriate gene for expression. A degenerate set of genes provides, in one mixture, all of the sequences encoding the desired set of potential soluble polypeptide sequences. The synthesis of degenerate oligonucleotides is well known in the art (see, e.g., Narang, Tetrahedron 39:3 (1983); Itakura et al., “Recombinant DNA,” (Proc. 3rd Cleveland Sympos. Macromolecules, ed. A G Walton, Amsterdam: Elsevier pp 273-289 (1981)); Itakura et al., Annu. Rev. Biochem. 53:323 (1984); Itakura et al., Science 198:1056 (1984); and Ike et al., Nucleic Acid Res. 11:477 (1983). Such techniques have been employed in the directed evolution of other proteins (see, e.g., Scott et al., Science 249:386-390 (1990); Roberts et al., Proc. Natl. Acad. Sci. U.S.A. 89:2429-2433 (1992); Devlin et al., Science 249:404-406 (1990); Cwirla et al., Proc. Natl. Acad. Sci. U.S.A. 87:6378-6382 (1990); and U.S. Pat. Nos. 5,223,409, 5,198,346, and 5,096,815).

Alternatively, other forms of mutagenesis can be utilized to generate a combinatorial library, including alanine scanning mutagenesis and the like (Ruf et al., Biochemistry 33:1565-1572 (1994); Wang et al., J. Biol. Chem. 269:3095-3099 (1994); Balint et al., Gene 137:109-118 (1993); Grodberg et al., Eur. J. Biochem. 218:597-601 (1993); Nagashima et al., J. Biol. Chem. 268:2888-2892 (1993); Lowman et al., Biochemistry 30:10832-10838 (1991); and Cunningham et al., Science 244:1081-1085 (1989)), linker scanning mutagenesis (Gustin et al., Virology 193:653-660 (1993); Brown et al., Mol. Cell Biol. 12:2644-2652 (1992); and McKnight et al., Science 232:316 (1982)); saturation mutagenesis (Meyers et al., Science 232:613 (1986)); by PCR mutagenesis (Leung et al., Methods Cell. Mol. Biol. 1:11-19 (1989)); or random mutagenesis, including chemical mutagenesis, (Miller et al., “A Short Course in Bacterial Genetics,” (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1992); and Greener et al., Strategies in Mol. Biol. 7:32-34 (1994)). Linker scanning mutagenesis, particularly in a combinatorial setting, is an attractive method for identifying truncated (bioactive) forms of the subject polypeptide.

A wide range of techniques are known in the art for screening gene products of combinatorial libraries made by point mutations and truncations, and for screening cDNA libraries for gene products having a certain property. Such techniques may be adapted for rapid screening of the gene libraries generated by the combinatorial mutagenesis of the subject semaphorin polypeptides. The most widely used techniques for screening large gene libraries typically comprise cloning the gene library into replicable expression vectors, transforming appropriate cells with the resulting library of vectors, and expressing the combinatorial genes under conditions in which detection of a desired activity facilitates relatively easy isolation of the vector encoding the gene whose product was detected. Some of the illustrative assays described herein (e.g., in the Example section, below) are amenable to high throughput analysis as necessary to screen large numbers of degenerate sequences created by combinatorial mutagenesis techniques.

In certain embodiments, the useful semaphorin molecules of the invention are small molecules such as a peptide and a peptidomimetic. As used herein, the term “peptidomimetic” includes chemically modified peptides and peptide-like molecules that contain non-naturally occurring amino acids, peptoids, and the like. Peptidomimetics provide various advantages over a peptide, including enhanced stability when administered to a subject. Methods for identifying a peptidomimetic are well known in the art and include the screening of databases that contain libraries of potential peptidomimetics. For example, the Cambridge Structural Database contains a collection of greater than 300,000 compounds that have known crystal structures (Allen et al., Acta Crystallogr. Section B 35:2331 (1979)). Where no crystal structure of a target molecule is available, a structure can be generated using, for example, the program CONCORD (Rusinko et al., J. Chem. Inf. Comput. Sci. 29:251 (1989)). Another database, the Available Chemicals Directory (Molecular Design Limited, Informations Systems; San Leandro Calif.), contains about 100,000 compounds that are commercially available and also can be searched to identify potential peptidomimetics of the semaphorin polypeptides.

In certain embodiments, the inhibitory and agonist semaphorin polypeptides of the invention may further comprise post-translational modifications. Such modifications include, but are not limited to, acetylation, carboxylation, glycosylation, phosphorylation, lipidation, and acylation. As a result, the modified soluble polypeptides may contain non-amino acid elements, such as polyethylene glycols, lipids, poly- or mono-saccharide, and phosphates. Effects of such non-amino acid elements on the functionality of a polypeptide can be tested using the functional assays described herein.

In certain aspects, functional variants or modified forms of the semaphorin polypeptides of the invention include fusion proteins having at least a portion of the semaphorin polypeptide and one or more fusion domains. Well known examples of such fusion domains include, but are not limited to, polyhistidine, Glu-Glu, glutathione S transferase (GST), thioredoxin, protein A, protein G, and an immunoglobulin heavy chain constant region (Fc), maltose binding protein (MBP), which are particularly useful for isolation of the fusion proteins by affinity chromatography.

For the purpose of affinity purification, relevant matrices for affinity chromatography, such as glutathione-, amylase-, and nickel- or cobalt-conjugated resins can be used. Another fusion domain well known in the art is green fluorescent protein (GFP). Fusion domains also include “epitope tags,” which are usually short peptide sequences for which a specific antibody is available. Well known epitope tags for which specific monoclonal antibodies are readily available include FLAG, influenza virus haemagglutinin (HA), and c-myc tags. In some cases, the fusion domains have a protease cleavage site, such as for Factor Xa or Thrombin, which allows the relevant protease to partially digest the fusion proteins and thereby liberate the recombinant proteins therefrom. The liberated proteins can then be isolated from the fusion domain by subsequent chromatographic separation. In certain embodiments, the soluble polypeptides contain one or more modifications that are capable of stabilizing the polypeptides. For example, such modifications enhance the in vivo (e.g., circulatory) half-life of the soluble polypeptides.

In one embodiment, an isolated or purified semaphorin protein can be immobilized on a suitable affinity matrix or solid support by standard techniques, such as chemical cross-linking (e.g., direct or through one or more linker molecules), or via an antibody raised against the protein or an affinity tag or via a ligand for an affinity tag. The solid support can be any suitable solid phase or matrix, such as a bead, the wall of a plate or other suitable surface (e.g., a well of a microtiter plate), column pore glass (CPG) or a pin that can be submerged into a solution, such as in a well. Conveniently the support may be made of e.g. glass, silica, latex, plastic or any polymeric material. The support may also be made from a biodegradable material. The surface of support may be hydrophobic or hydrophilic. The support may suitably have a functionalised surface. See, e.g., U.S. Pat. Nos. 4,336,173; 4,459,378; 4,654,267. A particulate support (e.g. beads or particles) may be substantially spherical. An example of a particulate support is monodisperse particles, i.e. such which are substantially uniform in size (e.g. size having a diameter standard deviation of less than 5%). Such have the advantage that they provide very uniform reproducibility of reaction. Non-magnetic polymer beads may also be applicable. Such are available from a wide range of manufactures, e.g. Dynal Particles AS, Qiagen, Amersham Biosciences, Serotec, Seradyne, Merck, Nippon Paint, Chemagen, Promega, Prolabo, Polysciences, Agowa, and Bangs Laboratories. Another example of a suitable support is magnetic beads or particles. Magnetic beads and particles may suitably be paramagnetic or superparamagnetic. Superparamagnetic beads and particles are e.g. described in EP 0106873. Magnetic beads and particles are available from several manufacturers, e.g. Dynal Biotech ASA.

The semaphorin molecules of the invention (e.g., agonist molecules) can be also attached, covalently or non-covalently, to one or more multimerization domain(s) such as, e.g., IgG or streptavidin. Useful organic molecule-based multimers include functionalized cyclic structures such as benzene rings and dextran. See, e.g., U.S. Pat. No. 5,635,363, US Patent Appl. Pub. No. 2004209295, PCT Publ. Nos. WO 02/072631 and WO 99/42597. Linkage to multimerization domains can be via covalent or non-covalent bonds, e.g., by chemical reactions between reactive groups of the multimerization domain (e.g. vinyl sulfone functionalities on a dextran polymer) and reactive groups on the semaphorin protein (e.g. amino groups on the protein surface), or by non-covalent interaction between a part of the semaphorin protein (e.g., a biotinylated peptide component) and the multimerization domain (e.g. four binding sites for biotin on the strepavidin tetrameric protein). Appropriate chemical reactions for the covalent coupling of semaphorins and the multimerization domain(s) include nucleophilic substitution by activation of electrophiles (e.g. acylation such as amide formation, pyrazolone formation, isoxazolone formation; alkylation; vinylation; disulfide formation), addition to carbon-hetero multiple bonds (e.g. alkene formation by reaction of phosphonates with aldehydes or ketones; arylation; alkylation of arenes/hetarenes by reaction with alkyl boronates or enolethers), nucleophilic substitution using activation of nucleophiles (e.g. condensations; alkylation of aliphatic halides or tosylates with enolethers or enamines), and cycloadditions. Appropriate molecules, capable of providing non covalent interactions between the one or more multimerization domain and the semaphorin protein, involve the following molecule pairs and molecules: streptavidin/biotin, avidin/biotin, antibody/antigen, DNA/DNA, DNA/PNA, DNA/RNA, PNA/PNA, LNA/DNA, leucine zipper e.g. Fos/Jun, IgG dimeric protein, IgM multivalent protein, acid/base coiled-coil helices, chelate/metal ion-bound chelate, streptavidin (SA) and avidin and derivatives thereof, biotin, immunoglobulins, antibodies (monoclonal, polyclonal, and recombinant), antibody fragments and derivatives thereof, leucine zipper domain of AP-1 (jun and fos), hexa-his (metal chelate moiety), hexa-hat GST (glutathione S-transferase) glutathione affinity, Calmodulin-binding peptide (CBP), Strep-tag, Cellulose Binding Domain, Maltose Binding Protein, S-Peptide Tag, Chitin Binding Tag, Immuno-reactive Epitopes, Epitope Tags, E2Tag, HA Epitope Tag, Myc Epitope, FLAG Epitope, AU1 and AU5 Epitopes, Glu-Glu Epitope, KT3 Epitope, IRS Epitope, Btag Epitope, Protein Kinase-C Epitope, VSV Epitope, lectins that mediate binding to a diversity of compounds, including carbohydrates, lipids and proteins, e.g. Con A (Canavalia ensiformis) or WGA (wheat germ agglutinin) and tetranectin or Protein A or G (antibody affinity). Combinations of such binding entities are also comprised. In particular, when the MHC complex is tagged, the multimerization domain(s) can be an “anti-tag”. By “anti-tag” is meant an antibody binding to the tag and any other molecule capable of binding to such tag. For multimerization techniques, see also Mekhaiel et al., Scientific Reports, 2011, 1:124.

Small Molecule Inhibitors and Agonists of the Invention

The present invention also encompasses small molecule inhibitors and agonists of Nrp1:semaphorin axis on Tregs. Small molecules are a diverse group of synthetic and natural substances generally having low molecular weights (preferably less than about 2000 Daltons, less than about 1000 Daltons, or less than about 500 Daltons). Small molecules, without limitation, may be, for example, nucleic acids, peptides, polypeptides, peptide nucleic acids, peptidomimetics, carbohydrates, lipids, or other organic (carbon containing) or inorganic molecules and may be synthetic or naturally occurring or optionally derivatized. Such small molecules may be a therapeutically deliverable substance or may be further derivatized to facilitate delivery or targeting. They can be isolated from natural sources (for example, plants, fungi, microbes and the like) or isolated from random or combinatorial chemical libraries of synthetic or natural compounds, or synthesized. See Werner et al., (2006) Brief Funct. Genomic Proteomic 5(1):32-6. Many random or combinatorial libraries are known in the art that can be used. Numerous means are currently used for random and directed synthesis of saccharide, peptide, and nucleic acid based compounds. Synthetic compound libraries are commercially available from Maybridge Chemical Co. (Trevillet, Cornwall, UK), Comgenex (Princeton, N.J.), Brandon Associates (Merrimack, N.H.), and Microsource (New Milford, Conn.). A rare chemical library is available from Aldrich (Milwaukee, Wis.). Alternatively, libraries of natural compounds in the form of bacterial, fungal, plant and animal extracts are available from e.g. Pan Laboratories (Bothell, Wash.) or MycoSearch (N.C.), or are readily producible. Additionally, natural and synthetically produced libraries and compounds are readily modified through conventional chemical, physical, and biochemical means (Blondelle et al., (1996) Tib Tech 14:60).

Methods for preparing libraries of molecules are well known in the art and many libraries are commercially available. Libraries of interest in the invention include peptide libraries, randomized oligonucleotide libraries, synthetic organic combinatorial libraries, and the like. Degenerate peptide libraries can be readily prepared in solution, in immobilized form as bacterial flagella peptide display libraries or as phage display libraries. Peptide ligands can be selected from combinatorial libraries of peptides containing at least one amino acid. Libraries can be synthesized of peptoids and non-peptide synthetic moieties. Such libraries can further be synthesized which contain non-peptide synthetic moieties, which are less subject to enzymatic degradation compared to their naturally-occurring counterparts. Libraries are also meant to include for example but are not limited to peptide-on-plasmid libraries, polysome libraries, aptamer libraries, synthetic peptide libraries, synthetic small molecule libraries and chemical libraries. The libraries can also comprise cyclic carbon or heterocyclic structure and/or aromatic or polyaromatic structures substituted with one or more of the above-identified functional groups.

Examples of chemically synthesized libraries are described in Fodor et al., (1991) Science 251:767-773; Houghten et al., (1991) Nature 354:84-86; Lam et al., (1991) Nature 354:82-84; Medynski, (1994) BioTechnology 12:709-710; Gallop et al., (1994) J. Medicinal Chemistry 37(9):1233-1251; Ohlmeyer et al., (1993) Proc. Natl. Acad. Sci. USA 90:10922-10926; Erb et al., (1994) Proc. Natl. Acad. Sci. USA 91:11422-11426; Houghten et al., (1992) Biotechniques 13:412; Jayawickreme et al., (1994) Proc. Natl. Acad. Sci. USA 91:1614-1618; Salmon et al., (1993) Proc. Natl. Acad. Sci. USA 90:11708-11712; PCT Publication No. WO 93/20242, dated Oct. 14, 1993; and Brenner et al., (1992) Proc. Natl. Acad. Sci. USA 89:5381-5383.

Examples of phage display libraries are described in Scott et al., (1990) Science 249:386-390; Devlin et al., (1990) Science, 249:404-406; Christian, et al., (1992) J. Mol. Biol. 227:711-718; Lenstra, (1992) J. Immunol. Meth. 152:149-157; Kay et al., (1993) Gene 128:59-65; and PCT Publication No. WO 94/18318.

Screening the libraries can be accomplished by any variety of commonly known methods. See, for example, the following references, which disclose screening of peptide libraries: Parmley and Smith, (1989) Adv. Exp. Med. Biol. 251:215-218; Scott and Smith, (1990) Science 249:386-390; Fowlkes et al., (1992) BioTechniques 13:422-427; Oldenburg et al., (1992) Proc. Natl. Acad. Sci. USA 89:5393-5397; Yu et al., (1994) Cell 76:933-945; Staudt et al., (1988) Science 241:577-580; Bock et al., (1992) Nature 355:564-566; Tuerk et al., (1992) Proc. Natl. Acad. Sci. USA 89:6988-6992; Ellington et al., (1992) Nature 355:850-852; U.S. Pat. Nos. 5,096,815; 5,223,409; and 5,198,346, all to Ladner et al.; Rebar et al., (1993) Science 263:671-673; and PCT Pub. WO 94/18318.

Identification and screening of agonists and antagonists of Nrp1:semaphorin axis can be further facilitated by determining structural features of the involved proteins, e.g., using X-ray crystallography, neutron diffraction, nuclear magnetic resonance spectrometry, and other techniques for structure determination. These techniques provide for the rational design or identification of agonists and antagonists.

Compounds Affecting Nrp1 or Semaphorin Expression or the Downstream Molecular Events in Tregs

As specified above, the present invention also encompasses inhibitors of Nrp1:semaphorin axis in Tregs which inhibit Nrp1 expression in Tregs, or locally (e.g., in tumors) inhibit semaphorin expression on conventional T cells, or prevent Nrp1 from engaging with its downstream signaling pathway(s).

The present invention also encompasses the agonists of Nrp1:semaphorin axis in Tregs which enhance Nrp1 expression in Tregs, or locally (e.g., in pancreatic islets for diabetes) enhance semaphorin expression on conventional T cells, or enhance Nrp1 engagement with its downstream signaling pathway(s).

Non-limiting examples of useful expression inhibitors include, e.g., interfering RNA (e.g., siRNA), dsRNA, RNA polymerase III transcribed DNAs, ribozymes, and antisense nucleic acids. Non-limiting examples of expression enhancement include, e.g., retroviral gene transfer, lentiviral gene transfer, overexpression using plasmids and transfection.

Antisense oligonucleotides, including antisense DNA, RNA, and DNA/RNA molecules, act to directly block the translation of mRNA by binding to targeted mRNA and preventing protein translation. For example, antisense oligonucleotides of at least about 15 bases and complementary to unique regions of the target DNA sequence can be synthesized, e.g., by conventional phosphodiester techniques (Dallas et al., (2006) Med. Sci. Monit. 12(4):RA67-74; Kalota et al., (2006) Handb. Exp. Pharmacol. 173:173-96; Lutzelburger et al., (2006) Handb. Exp. Pharmacol. 173:243-59).

siRNA comprises a double stranded structure typically containing 15 to 50 base pairs and preferably 21 to 25 base pairs and having a nucleotide sequence identical or nearly identical to an expressed target gene or RNA within the cell. Antisense polynucleotides include, but are not limited to: morpholinos, 2′-O-methyl polynucleotides, DNA, RNA and the like.

RNA polymerase III transcribed DNAs contain promoters, such as the U6 promoter. These DNAs can be transcribed to produce small hairpin RNAs in the cell that can function as siRNA or linear RNAs that can function as antisense RNA. The inhibitor may be polymerized in vitro, recombinant RNA, contain chimeric sequences, or derivatives of these groups. The inhibitor may contain ribonucleotides, deoxyribonucleotides, synthetic nucleotides, or any suitable combination such that the target RNA and/or gene is inhibited. In addition, these forms of nucleic acid may be single, double, triple, or quadruple stranded. (see for example Bass (2001) Nature, 411, 428 429; Elbashir et al., (2001) Nature, 411, 494 498; and PCT Publication Nos. WO 00/44895, WO 01/36646, WO 99/32619, WO 00/01846, WO 01/29058, WO 99/07409, WO 00/44914).

Ribozymes are enzymatic RNA molecules capable of catalyzing the specific cleavage of RNA. The mechanism of ribozyme action involves sequence specific hybridization of the ribozyme molecule to complementary target RNA, followed by endonucleolytic cleavage. Engineered hammerhead motif ribozyme molecules that specifically and efficiently catalyze endonucleolytic cleavage of mRNA sequences are also within the scope of the present invention. Scanning the target molecules for ribozyme cleavage sites that include the following sequences, GUA, GUU, and GUC initially identifies specific ribozyme cleavage sites within any potential RNA target. Once identified, short RNA sequences of between about 15 and 20 ribonucleotides corresponding to the region of the target gene containing the cleavage site can be evaluated for predicted structural features such as secondary structure that may render the oligonucleotide sequence unsuitable. The suitability of candidate targets can also be evaluated by testing their accessibility to hybridization with complementary oligonucleotides using, e.g., ribonuclease protection assays.

Expression inhibitors of the present invention can be prepared by known methods. These include techniques for chemical synthesis such as, e.g., by solid phase phosphoamite chemical synthesis. Alternatively, antisense RNA molecules can be generated by in vitro or in vivo transcription of DNA sequences encoding the RNA molecule. Such DNA sequences can be incorporated into a wide variety of vectors that incorporate suitable RNA polymerase promoters such as the T7 or SP6 polymerase promoters. See, e.g., Weintraub, H. et al., Antisense RNA as a molecular tool for genetic analysis, Reviews—Trends in Genetics, Vol. 1 (1) 1986.

Various modifications to the oligonucleotides of the present invention can be introduced as a means of increasing intracellular stability and half-life. Possible modifications include but are not limited to the addition of flanking sequences of ribonucleotides or deoxyribonucleotides to the 5′ and/or 3′ ends of the molecule, or the use of phosphorothioate or 2′-O-methyl rather than phosphodiesterase linkages within the oligonucleotide backbone.

Aptamers nucleic acid sequences are readily made that bind to a wide variety of target molecules. The aptamer nucleic acid sequences of the invention can be comprised entirely of RNA or partially of RNA, or entirely or partially of DNA and/or other nucleotide analogs. Aptamers are typically developed to bind particular ligands by employing known in vivo or in vitro (most typically, in vitro) selection techniques known as SELEX (Systematic Evolution of Ligands by Exponential Enrichment). Methods of making aptamers are described in, for example, Ellington and Szostak (1990) Nature 346:818, Tuerk and Gold (1990) Science 249:505, U.S. Pat. No. 5,582,981; PCT Publication No. WO 00/20040; U.S. Pat. No. 5,270,163; Lorsch and Szostak (1994) Biochem. 33:973; Mannironi et al., (1997) Biochem. 36:9726; Blind (1999) Proc. Nat'l. Acad. Sci. USA 96:3606-3610; Huizenga and Szostak (1995) Biochem. 34:656-665; PCT Publication Nos. WO 99/54506, WO 99/27133, and WO 97/42317; and U.S. Pat. No. 5,756,291.

In one specific embodiment, the inhibitor of Nrp1:semaphorin axis inhibits a signaling pathway between the cytoplasmic domain of Nrp1 protein comprising the C-terminal amino acid sequence SEA (C-terminal PDZ domain-binding motif) and PTEN protein; such inhibitor can be, e.g., a peptide or a small molecule or a fragment of Nrp1 protein comprising all or part of its cytoplasmic domain comprising the C-terminal amino acid sequence SEA or a derivative or an analog thereof.

Methods for Administering Compositions Comprising Inhibitors or Agonists of the Invention

In certain embodiments, the inhibitors and agonists of the invention are formulated in pharmaceutical compositions with a pharmaceutically acceptable carrier or excipient. The compounds can be formulated for administration in any convenient way for use in human or veterinary medicine. Wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, release agents, coating agents, preservatives and antioxidants can also be present in the compositions.

The formulations may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art. The amount of active ingredients that can be combined with a carrier material to produce a single dosage form will vary depending upon the host being treated and the particular mode of administration. The amount of active ingredients that can be combined with a carrier material to produce a single dosage form will generally be that amount of the compound which produces a therapeutic effect.

In general, the formulations can be prepared with a liquid carrier, or a finely divided solid carrier, or both, and then, if necessary, shaping the product.

Formulations for oral administration may be in the form of capsules, cachets, pills, tablets, powders, granules, or as a solution or a suspension in an aqueous or non-aqueous liquid, or as anoil-in-water or water-in-oil liquid emulsion, and the like, each containing a predetermined amount of one or more active ingredients.

In solid dosage forms for oral administration (capsules, tablets, pills, dragees, powders, granules, and the like), one or more active ingredients can be mixed with one or more pharmaceutically acceptable carriers, such as sodium citrate or dicalcium phosphate, and/or any of the following: (1) fillers or extenders, such as starches, lactose, sucrose, glucose, mannitol, and/or silicic acid; (2) binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose, and/or acacia; (3) humectants, such as glycerol; (4) disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; (5) solution retarding agents, such as paraffin; (6) absorption accelerators, such as quaternary ammonium compounds; (7) wetting agents, such as, for example, cetyl alcohol and glycerol monostearate; (8) absorbents, such as kaolin and bentonite clay; (9) lubricants, such a talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof; and (10) coloring agents. In the case of capsules, tablets and pills, the pharmaceutical compositions may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like.

Suspensions, in addition to one or more active ingredients, can contain suspending agents such as ethoxylated isostearyl alcohols, polyoxyethylene sorbitol, and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.

Compositions of the invention can be also administered topically, either to skin or to mucosal membranes. This offers the greatest opportunity for direct delivery with the lowest chance of inducing side effects. The topical formulations may further include one or more of the wide variety of agents known to be effective as skin or stratum corneum penetration enhancers. Examples of these are 2-pyrrolidone, N-methyl-2-pyrrolidone, dimethylacetamide, dimethylformamide, propylene glycol, methyl or isopropyl alcohol, dimethyl sulfoxide, and azone. Additional agents may further be included to make the formulation cosmetically acceptable. Examples of these are fats, waxes, oils, dyes, fragrances, preservatives, stabilizers, and surface active agents. Keratolytic agents such as those known in the art may also be included. Examples are salicylic acid and sulfur.

Dosage forms for the topical or transdermal administration include powders, sprays, ointments, pastes, creams, lotions, gels, solutions, patches, and inhalants. The subject therapeutic agents may be mixed under sterile conditions with a pharmaceutically acceptable carrier, and with any preservatives, buffers, or propellants which may be required. The ointments, pastes, creams and gels may contain, in addition to a subject polypeptide agent, excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to one or more active ingredients, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates, and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane.

Pharmaceutical compositions suitable for parenteral administration may comprise one or more active ingredients in combination with one or more pharmaceutically acceptable sterile isotonic aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents. Examples of suitable aqueous and nonaqueous carriers which may be employed in the pharmaceutical compositions of the disclosure include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.

These compositions can also contain preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption, such as aluminum monostearate and gelatin.

Injectable depot forms can be made by forming microencapsule matrices of one or more active ingredients in biodegradable polymers such as polylactide-polyglycolide. Depending on the ratio of active ingredient to polymer, and the nature of the particular polymer employed, the rate of antagonist release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the antagonists in liposomes or microemulsions which are compatible with body tissue.

Formulations for intravaginal or rectal administration may be presented as a suppository, which may be prepared by mixing one or more active ingredients with one or more suitable nonirritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate, and which is solid at room temperature, but liquid at body temperature and, therefore, will melt in the rectum or vaginal cavity and release the active compound.

EXAMPLES

The present invention is also described and demonstrated by way of the following examples. However, the use of these and other examples anywhere in the specification is illustrative only and in no way limits the scope and meaning of the invention or of any exemplified term. Likewise, the invention is not limited to any particular preferred embodiments described here. Indeed, many modifications and variations of the invention may be apparent to those skilled in the art upon reading this specification, and such variations can be made without departing from the invention in spirit or in scope. The invention is therefore to be limited only by the terms of the appended claims along with the full scope of equivalents to which those claims are entitled.

Example 1 Materials and Methods

Mice.

C57/BL6 and dnTGFβRII mice were purchased from the Jackson Laboratories. Foxp3^(YFP-iCre), Foxp3⁻ and Foxp3^(DTR-gfp) mice were obtained from A.Y. Rudensky (HHMI/Washington University; see Rubtsov et al., Immunity, 2008, 28:546-558; Fontenot et al., Nat Immunol., 2003, 4(4):330-336; Kim et al., Nat Immunol., 2007, 8(2):191-197). Il10^(−/−) mice were obtained from T. Geiger (St. Jude Children's Research Hospital; see Selvaraj and Geiger, J Immunol., 2008, 180(5):2830-2838). Nrp1^(f/f) mice were obtained from D. Cheresh (UCSD; see Acevedo et al., Blood, 2008, 111(5):2674-2680). Foxp3⁻×CD45.1 mice were bred from heterozygous crosses. Animal experiments were performed in American Association for the Accreditation of Laboratory Animal Care-accredited, specific-pathogen-free facilities in the St. Jude Animal Resource Center. Animal protocols were approved by the St Jude Animal Care and Use Committee.

Nrp1 and Semaphorin Antibodies.

Mouse Sema-3a, mouse Nrp1 and human Sema4a-Ig were purchased from R&D Biosystems. Two different Nrp1 blocking antibodies were used in the experiments: (i) R&D AF566 are anti-Nrp1 mouse/rat affinity purified polyclonal antibodies (Goat IgG), and (ii) anti-Nrp1 monoclonal antibodies (Rat IgG2a), provided by R&D Biosystems (R&D Systems, clone 761704, MAB59941). The following antibodies to semaphorin-4a (Sema4a) were used: clone 5E3 from MBL International and monoclonal antibodies from R&D Biosystems (clone 757129) (see, e.g., FIGS. 1E, 2H, 4I). Sema4a staining antibody was purchased from MBL International (clone 5E3), and conjugated to biotin or Alexa Fluor 647 in-house. Most flow cytometric antibodies were purchased from BioLegend. Anti-Foxp3 and anti-Eomes were purchased from eBioscience. KLF2 antibody was purchased from Millipore. Phospho-Akt (S473), phospho-S6K1 (T421/5424), Foxo3a, and pan Akt antibodies were purchased from Cell Signaling Technologies. PTEN-HRP antibody was purchased from Santa Cruz Biotechnology.

RNA interference. Control siRNA (Catalog #4390843) and pools of Sema4a (Catalog #4390771, siRNA# s73547) siRNA were purchased from Life Technologies and resuspended per the manufacturer's instructions. CD4⁺ and CD8⁺ conventional T cells were sorted magnetically by negative selection and transfected by Amaxa (Lonza) with 300 pMol siRNA and 2 μg of pMaxGFP control plasmid, rested overnight in Amaxa nucleofector media. Cells were then sorted based on GFP, CD25, and CD45RB expression and cocultured with Treg cells in the top well of a transwell suppression assay.

Plasmids.

Nrp1.mCherry was obtained from Addgene and used as a template to generate retroviral overexpresion constructs. Nrp1^(WT) was generated by adding the native signal sequence and cloned into pMlCherry. Nrp1^(ΔSEA) was generated from the WT construct, deleting the terminal SEA motif by mutation of the serine codon to a stop codon. Akt^(WT), Akt^(DN) (dominant-negative kinase dead K179M as described by Franke et al., Cell, 1995, 81:727-736), and pBabe empty vector were obtained from D. R. Green (described in Morgenstern J P, Land H., 1990, Nucleic Acids Research 18(12):3587-96).

Human T Cell Populations.

Human umbilical cord samples were provided by B. Triplett, M. Howard and M. McKenna at the St. Louis Cord Blood Bank, and were obtained from the umbilical vein immediately after vaginal delivery with the informed consent of the mother and approved by St. Louis Cord Blood Bank Institutional Review Board (IRB). Research use approved by the St. Jude IRB.

Transwell Suppression.

1.25×10⁴ Treg purified by FACS (CD45RB^(lo) Foxp3^(YFP-iCre+)) were stimulated in the top chamber of a Millipore Millicell 96 (0.4 μm pore size) in the presence of sorted Tconv (CD45RB^(hi) CD25⁻CD4⁺ or CD8⁺), B cells (B220⁺), or Treg at a 1:4 ratio, Sema4a-Ig or IgG-conjugated latex beads (1:1 ratio), anti-CD3 (145.2C11) and anti-CD28 (37.51) (obtained from BioLegend) conjugated latex beads (purchased from Life Technologies) (1:1 ratio), and/or neutralizing antibodies. In some experiments, the top well co-cultured cells were fixed with 2% PFA for 15 minutes and washed extensively before co-culture with Treg. 2.5×10⁴ purified Treg were stimulated in the bottom well with anti-CD3/anti-CD28 beads at a 1:1 ratio. Cells were cultured for 72 hours and pulsed with ³[H]-thymidine for the final 8 hours. The bottom chambers were harvested and read with a beta counter.

For human studies, sorted umbilical cord blood Tconv (CD4⁺CD25) and Treg (CD4⁺CD25⁺) were activated with 3 μg/mL plate-bound anti-CD3 (clone OKT3, Biolegend), 2 μg/mL soluble anti-CD28 (clone CD28.1, Biolegend), and 100 U/mL rhIL-2 (St. Jude Pharmacy) for 7-9 days. After harvesting and washing, Treg were stimulated at a 1:200 ratio with fixed autologous Tconv or IgG/Sema4a-Ig coated latex beads in the top well of a transwell plate. 2.5×10⁴ Tconv were stimulated in the bottom well at a 1:1 ratio with OKT3/CD28.1 coated latex beads. Cells were cultured for 5 days and pulsed with ³[H]-thymidine for the final 8 hours. The bottom chambers were harvested and read with a beta counter.

“Percent transwell suppression” is defined as 100−100×[(CPM of a particular well)/(Average CPM of unsuppressed cells)] to normalize across experiments.

Fusion Proteins. The sequence encoding the extracellular domains of Sema4a or Nrp1 was cloned in-frame to pX-Ig to create a Sema4a- or Nrp1-mouse IgG1-Fc fusion protein construct (Sema4a-Ig or Nrp1-Ig). J558L B cells were electroporated with this construct, and high producing clones were selected by single-cell sorting. High producing clones were seeded into Sartorious Bioreactors and harvested for protein G purification and concentration. Sulfate latex 4 μm beads (Life Technologies) were conjugated with isotype control (mouse IgG1, MOPC21, R&D Biosystems) or Sema4a-Ig overnight with 3 pg protein per bead, blocked with 10% FBS, and stored in media. Mouse Sema-3a-Fc, Sema4a-Fc, mouse Nrp1, and human Sema4a-Fc were purchased from R&D Systems.

Binding Assays.

High protein binding plates were coated with 500 ng/mL recombinant murine Nrp1 (R&D Systems) overnight in PBS. After a 1-2 h block in 1% BSA in PBS at room temperature, coated plates were incubated with various concentrations of Sema4a-Ig or mouse IgG1 for 2-4 hours in the presence of anti-Sema4a, anti-Nrp1, or isotype control antibodies. Plates were then washed with PBS+0.05% TWEEN-20 10 times and incubated with 500 ng/mL biotinylated anti-mouse IgG1 antibody (BD Biosciences) to bind the fusion protein (or mouse IgG1 control). After 7 washes, Strepdavidin-HRP (GE Healthcare) was added at 500 ng/mL to detect the biotinylated antibody. After another 7 washes, TMB substrate (Thermo Scientific) was added and stopped with 1N H₂SO₄.

For VEGF binding, the same protocol was followed, except rather than Sema4a-Ig being used, VEGF165 (R&D Systems) was used at 50 ng/mL in PBS and detected with 500 ng/mL anti-VEGF-biotin (R&D Systems) followed by SA-HRP for detection. For comparisons across Sema family members, plates were coated with varying concentrations of Sema3a-Fc, Sema4d-Fc, Sema4a-Ig, or isotype control overnight. Biotinylated Nrp1-Ig was added and incubated for 3 hours, and SA-HRP was used for detection.

mRNA analysis.

RNA was extracted from cells lysed in TRIzol reagent (Life Technologies) and reverse transcribed with the High Capacity Reverse Transcription kit (Applied Biosystems). Real-time PCR was performed using primers and probes and TaqMan master mix or SYBR green chemistry (Applied Biosystems).

Rescue of Foxp3-Deficient Autoimmunity.

CD45.1×Foxp3^(+/−) female mice were bred to CD45.1 male mice in timed breedings. Male progeny were genotyped at birth for Foxp3⁻ status. 1×10⁶ purified Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) CD45.2⁺ Tregs, purified by flow cytometry, were injected intraperitoneally into Foxp3⁻ male pups within 3 days of birth. Mice were monitored for the scurfy phenotype (scaly skin, eye inflammation, runted phenotype, and lack of mobility). For some experiments, all mice were sacrificed at 5 weeks for histological analysis of the ear pinna, liver, and lung.

Tumor Models.

Foxp3^(Cre), Nrp1^(f/f)Foxp3^(Cre), or Foxp3^(DTR.gfp) mice were injected with B16.F10 melanoma (1.25×10⁵ cells i.d.), EL4 thymoma (1.25×10⁵ cells i.d.), or MC38 colon carcinoma (2.5×10⁵ cells s.c.). Tumors were measured regularly with digital calipers and tumor volume calculated. Tumors and lymph nodes were harvested for analysis. TILs were prepared using a Percoll gradient from tumor samples after mechanical disruption. For metastasis studies, B16.F10 was injected intravenously at various doses. After 17-20 days, lungs were harvested, inflated with H₂O₂, and metastases were counted. Therapeutic B16 experiments were conducted by injecting 1.25×10⁵ B16 melanoma cells i.d. and waiting until tumors were palpable (5 days). On day 5, mice began receiving intraperitoneal injections of either rat IgG2a or anti-Nrp1 (R&D Systems, clone 761704) (400 μg initial dose and 200 μg every three days).

Experimental Colitis.

6-to-8 week old RAG2^(−/−) mice were injected intraperitoneally with 4×10⁵ congenitally marked CD45RB^(hi) CD25⁻ Tconv cells. 21 to 28 days later (when the majority of the mice had lost 5% body weight and had colitis symptoms), 1×10⁶ Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) Treg were injected intraperitoneally. Body weight was measured daily, and 28 days after Treg rescue, sections were stained for histology.

Signaling Analysis.

For flow cytometry, Treg were stimulated with anti-CD3e/anti-CD28 coated beads and either purified conventional T cells or Sema4a-Ig beads for various times, then fixed with 1% PFA for 15 minutes at 37° C. Cells were then permeabilized in ice-cold 90% MeOH for 20 min at −20° C. After extensive washing in PBS, cells were blocked with 10% normal mouse serum in PBS for 10 minutes at RT. Cells were then stained with antibodies in 1% BSA in PBS (pAkt (T308), pAkt (S473)) for 1 hour at RT in the dark. Finally, cells were stained with appropriate secondary antibodies for 30 minutes at RT in the dark, then washed and analyzed. For immunoblot analysis, Treg were expanded with 1 ng/mL phorbol-13-myristol acetate and 10 ng/mL ionomycin with 500 U rhIL-2 for 3 days, then washed extensively with media, and expanded to 10× volume in 500 U rhIL-2. After an overnight rest with no IL-2, Treg were stimulated with plate-bound anti-CD3, soluble anti-CD28 and bead-bound Sema4a-Ig for 3 hours, then lysed in whole cell lysis buffer (1% NP40, 5 mM EDTA, 5 mM EGTA, TWEEN-20) for 15 min on ice. In some experiments, 3×10⁶ Treg were lysed in a larger volume, and cleared lysates were incubated with Protein G beads for 3 hours to “preclear” the lysate. Nrp1 was immunoprecipitated using a polyclonal anti-Nrp1 antibody (R&D AF566) overnight followed by a 3 hour incubation with Protein G beads. Beads were washed with lysis buffer before elution and reduction prior to immunoblotting. Briefly, precipitates or input lysates were incubated at 100° C. with 2-mercapto-ethanol and 4×LDS sample buffer (Life Technologies), then loaded into 4-12% Bis-Tris NuPAGE gels (Life Technologies), and run for 1 hour at 200V. Separated gels were electrotransferred to PVDF membranes using the Criterion Gel Blotting System (Biorad), and blocked for 1 hour at room temperature with 3% BSA in TBS supplemented with 0.1% TWEEN20. Blocked membranes were incubated overnight with anti-PTEN directly conjugated to HRP, washed three times with TBS-TWEEN, and imaged using Western Lightning ECL.

Retroviral Transduction.

293T cells were transfected with pPAM-EQ and pVSV-G packaging plasmids with various retroviral constructs to transduce GPE86 retroviral producer cells. Treg cells were purified flow cytometrically. Treg were activated and cycled with PMA and ionomycin in the presence of 500 U/mL rhIL-2 for 24 h in 96 well flat bottom plates at 5×104 per well in 100 μL. Viral supernatants were concentrated using 100 kDa MWCO concentrators (Millipore) 10 fold and added in equal volume to cycling Treg cells in the presence of 500 U/mL rhIL-2 and 6 μg/mL polybrene and centrifuged at 2500 rpm for 60 min at 37 deg, then incubated for 24 h. The spinduction process was repeated twice every 24 h, removing 100 μL of supernatant from the cultured Treg each day to keep the culture volume at 200 μL per well. Treg cells were then washed in media and sorted based on fluorescent protein expression or selected with 1 μg/mL puromycin and expanded further in IL-2. Fluorescent protein or intracellular epitope staining (anti-HA, Sigma) was confirmed prior to use. Functional assays were performed after a 24 h rest without IL-2.

Microscopy.

TIRF illumination of IS activation was performed as previously described⁵⁰. Briefly, lipid bilayers containing anti-TCR and an anti-mouse IgG1 capture antibody loaded with Sema4a-Ig or isotype control were prepared. Treg cells were stimulated on the bilayer for 20 minutes, then fixed, permeabilized, and stained for phospho-Akt (S473), global phosphotyrosine (4G10), or Nrp1. “Percentage of pAkt+ TCR clusters” represents the ratio of phosphorylated Akt (S473) positive synapses to the total number of synapses formed as read-out by TCR clustering. Foxo3a was performed on freshly isolated Treg left unstimulated in media overnight or stimulated with immobilized anti-CD3/anti-CD28 in the presence or absence of immobilized Sema4a-Ig or its isotype control. Cells were harvested, fixed in 1% PFA, and permeabilized with 0.1% Triton X-100 in TBS. After blocking with normal mouse serum, cells were stained with anti-Foxo3a (Cell Signaling Technologies) overnight in Tris-buffered 1% BSA. After several washes, cells were stained with Alexa Fluor 647 conjugated anti-rabbit IgG (Life Technologies), and then washed several times. Cells were then loaded with DAPI and phalloidin-Alexa Fluor 546 or 488 prior to microscopy. Random fields of 10-30 cells were visualized using spinning-disc laser scanning confocal microscopy. Blinded masks were generated using phalloidin and DAPI staining to determine cytoplasmic and nuclear volume, respectively, and only then was the Foxo3a staining visualized. The nuclear and cytoplasmic volumes of Foxo3a fluorescence of 20-30 stacks were calculated using Slidebook (3i, Inc.) software in arbitrary fluorescence units and analyzed in Graphpad Prism.

Affymetrix Array and Analysis.

Foxp3^(Cre) or Nrp1^(f/f)Foxp3^(Cre) Treg were flow cytometrically sorted to 99.0% purity from 6-8 week old mice, and stimulated 48 hours with plate-bound anti-CD3, anti-CD28, 100 U/mL rhIL-2, and either isotype or Sema4a-Ig coated latex beads. Cells were harvested, washed three times with PBS, and lysed in TRIzol reagent (Life Technologies). Quality was confirmed by UV spectrophotometry and by analysis on an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, Calif.). Total RNA (100 ng) was processed and labeled in the Hartwell Center for Biotechnology & Bioinformatics according to the Affymetrix 3′ IVT Express protocol and arrayed on a mouse high throughput 430 PM GeneChip array. Signal data was RMA summarized, visualized, quality checked by principal component analysis (PCA) (Partek Genomics Suite 6.6 St Louis Mo., USA). Batch correction was applied as needed to correct differences in completely replicated experiments scanned on distinct dates. To compare Tconv cells to resting Tregs and unequal variance t test was applied to each probeset and the log 2ratio calculated. This same analysis was used to compare T cony cells to activated Treg cells. To compare the effect of Sema4a treatment in wild-type Treg cells to the effect of sema treatment in Nrp1-deficient cells a two factor ANOVA interaction of treatment and genotype was applied to each probeset and the Storey q value was found to correct for multiple comparisons. The categorical mean of each probeset was found, transformed to a Z-score, hierarchically clustered and visualized by heat-map in Spotfire DecisionSite 9.1 (Tibco, Somerville MA, USA) (FIG. 1A). The heat map in FIG. 11B was composed of the top named genes that had the passed p value interaction FDR at 10%, had a minimum mean expression of 6 in one class and a minimum absolute value logratio difference of at least 0.5. The volcano plots were generated using STATA/SE 11.1 (College Station Tex., USA). For all volcano plots genes without official symbols or names were removed. In these plot score refers to the −log base 10 transformed p value. For the interaction volcano plot genes a metric for distance from the origin was applied to color code the graph |(score/10+|logratio difference|)/2|>0.5. Statistical tests and multiple comparison corrections were performed using Partek Genomics Suite 6.6 (St Louis Mo., USA). Sequences were retrieved for probesets that had at least a 3 fold difference between Tconv and activated Treg cells and a p value of 0.01 and these sequences were then tested with SignalP 3.0 software to identify transmembrane domains.

Results

Semaphorin 4a is a Tconv-Expressed Ligand that Stimulates Treg Activity

The present inventors and co-workers have previously suggested that the transcriptional and functional profile of Tregs stimulated in the presence or absence of co-cultured conventional CD4⁺ T cells (Tconv) is markedly different^(12,13). Tregs can only suppress Tconv across a permeable Transwell membrane when in direct contact with Tconv placed in the top chamber (referred to herein as Transwell suppression), suggesting a contact-dependent mechanism that enhances Treg function¹². The present inventors sought to determine the signals that induce this distinct Treg activity and transcriptional profile. They hypothesized that Tregs could not ‘self-boost’ suggesting that the ligand that mediates this activity may be expressed by Tconv but not by Tregs. Indeed, Treg stimulated alone or in co-cultured with additional live or fixed Foxp3⁺ Tregs or B220⁺ B cells could not mediate suppression across a Transwell membrane in a Transwell suppression assay of Tconv stimulated with anti-CD3/anti-CD28 coated beads in the bottom well when regulatory T cells (Tregs) were stimulated in the top well (FIG. 1A). In contrast, Tregs co-cultured with fixed CD4⁺ or CD8⁺ T cells could potentiate Transwell suppression, suggesting that the ligand was cell-surface expressed¹². Gene expression was compared between resting and activated Treg and CD4⁺ Tconv cells using Affymetrix analyses of Tconv and Treg populations sorted from Foxp3.GFP mice and incubated together or separately with irradiated APC in the presence or absence of anti-CD3 antibody (after 48 hours, RNA extracted from cells re-sorted based on CD4 and GFP expression was subjected to Affymetrix analysis). This list was curated to focus on gene encoding cell surface-expressed proteins that were predominantly expressed by Tconv. From this list, the top three genes, Sema4a (semaphorin-4a), Tgfbr3 (transforming growth factor, beta receptor III) and Itgb3 (integrin beta 3; CD61), were selected for further study based on previous studies implicating their roles in immunoregulation and confirmation of their differential expression in CD4⁺ Tconv cells versus Tregs and B220⁺ B cells by qPCR. Whereas Sema4a and Tgfbr3 were also enhanced in CD8⁺ T cells, Itgb3 was not. The inventors then sought to identify a cell line that could be used to assess the capacity of these molecules to potentiate Treg function. It was found that 3T3 fibroblasts expressed high amounts of Tgfbr3 and Itgb3 but could not mediate Treg boosting. In contrast 3T3 cells did not express Sema4a. Taken together, these data suggested that Sema4a, which has been shown to modulate axon activity and immune regulation¹⁴, warranted further investigation.

Four approaches were used to determine if Sema4a was required and sufficient to potentiate Treg function.

First, dose-dependent inhibition of Treg boosting by Tconv in a Transwell suppression assay was observed with a Sema4a blocking mAb (clone 5E3, MBL International) (FIG. 1B). Second, siRNA knockdown of Sema4a expression in CD4⁺ and CD8⁺ Tconv cells limited their ability to boost Treg suppression. This was determined (i) in a Transwell suppression assay after CD4⁺ or CD8⁺ Tconv were mock transfected or transfected with scrambled siRNA or Sema4a siRNA and (ii) after CD4⁺ and CD8⁺ T cells enriched using negative magnetic separation and nucleofected with 200 pM scrambled (siControl) or a pool of 3 Sema4a-targeting (Life Technologies Catalog #4390771, siRNA# s73547) (siSema4a) siRNA were resorted and stimulated 16 hours after transfection with anti-CD3 and anti-CD28 for 24 hours followed by RNA extraction and performing qPCR for Sema4a mRNA (FIG. 1C).

Third, whereas Sema4a loss variants of the 3A9 T cell hybridoma failed to boost Treg function in a Transwell assay, Sema4a⁺ clones or Sema4a transfectants of the Sema4a loss variant potentiated Treg suppression (FIG. 4). Sema4a 3T3-transfectants (transduced with a retrovirus expressing a Sema4a overexpression construct), but not empty vector control cells, also potentiated Treg Transwell suppression.

Fourth, a murine Sema4a-Ig fusion protein, but not an IgG1 isotype control, coated on to beads was sufficient to induce potent Transwell suppression to an extent equivalent to Tconv cells (FIG. 1D).

In addition, an anti-Sema4a antibody showed dose-dependent inhibition of T_(reg) potentiation (FIG. 1E). It was then assessed if other immune cells expressed Sema4a. While CD4⁺ and CD8⁺ T cells displayed low but demonstrable Sema4a expression, lymph node CD11c⁺ dendritic cells (DCs) and DX5⁺ natural killer cells appeared to express high levels of Sema4a (as determined in peripheral spleen/lymph node preparations stained with anti-Sema4a and analyzed flow cytometrically). Interestingly, lymph node CD11c⁺ DCs could potentiate T_(reg) suppression in Sema4a-dependent manner (FIG. 1E).

It was next determined if Sema4a was sufficient to potentiate T_(reg) function. Sema4a 3T3-transfectants, but not empty vector control cells, could potentiated T_(reg) Transwell suppression. Importantly, a murine Sema4a-Ig fusion protein, but not an IgG1 isotype control, coated onto beads was sufficient to induce Transwell suppression to an extent equivalent to T_(conv) cells (FIG. 1D).

Collectively, these data suggest that Sema4a is required and sufficient to potentiate Treg function in vitro.

Nrp-1 is aSema4a Receptor Required to Boost Treg Function and Survival

Neuropilin-1 (Nrp1) is a co-receptor for a class III semaphorin, Sema3a, with key roles in controlling axonal guidance¹⁵. Nrp1 induces axon growth cone collapse, preventing infiltration into privileged tissues and genetic deletion in mice results in embryonic lethality¹⁶. Nrp1 has also been shown to interact with vascular-endothelial growth factor (VEGF), platelet derived growth factor beta (PDGFβ) and transforming growth factor beta (TGFβ)^(17,18). Nrp1 has been shown to be highly expressed in Tregs and is a useful marker, especially in thymically derived “natural” Treg (as determined by flow cytometric analysis of Foxp3 and neuropilin expression in CD4⁺ T cells in Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) mice)¹⁹⁻²¹. Although a role for Nrp1 in T cells has been implicated²², no role for Nrp1 in Tregs has been identified.

The present inventors postulated that Nrp1 may be the receptor for Sema4a that mediates Treg functional potentiation. First, an Nrp1-specific mAb could block Treg boosting in vitro (FIG. 2A). Direct interaction between Sema4a and Nrp1 was verified in an ELISA assay with purified, recombinant Nrp1 and Sema4a (FIG. 2H). Importantly, dose-dependent inhibition was observed with Nrp1 and Sema4a mAbs that disrupt Nrp1:Sema, but not Nrp1:VEGF, interaction (FIG. 2H). Second, Nrp1-deficient Tregs, generated by crossing Nrp1^(f/f) and Foxp3^(Cre) mice (herein referred to as Nrp1^(f/f)Foxp3^(Cre))^(17,23), lacked cell surface Nrp1 expression and failed to mediate Transwell suppression following co-culture with Tconv cells or Sema4a-Ig-coated beads (FIG. 2B). However, Nrp1-deficient Tregs retained the capacity to mediate contact-dependent suppression (as determined by classical suppression assay in which wild-type or neuropilin-deficient Tregs were cocultured different concentrations in the presence of anti-CD3/anti-CD28 coated beads). Importantly, direct interaction between Sema4a and Nrp1 was verified by flow cytometric staining of Foxp3^(Cre), but not Nrp1^(f/f)Foxp3^(Cre), Tregs with fluorochrome-labeled Sema4a-Ig and in an ELISA assay with purified, recombinant Nrp1 and Sema4a, which appeared equivalent to its known ligand Sema3a. While these data clearly demonstrate that Sema4a can bind to Nrp1 and boost Treg function, it is possible that other semaphorin family members could also serve this function. Second, an Nrp1-specific mAb blocked Treg Transwell suppression in vitro (FIG. 2I).

The present inventors and co-workers have previously shown that Tregs mediate Transwell suppression via IL-10 and IL-35 but not TGFβ¹². Herein, two experimental approaches were used to determine if the mechanisms used by Tconv cell- and Sema4a-boosted Tregs to suppress were synonymous. First, Tregs stimulated in the presence of Sema4a-Ig-coated beads in the top chamber of a Transwell plate were equally capable of suppressing wild-type (WT) and dnTGFβRII Tconv cells, which are insensitive to TGFβ²⁴, in the bottom chamber suggesting that TGFβ is not required (FIG. 2C). In contrast, Il10^(−/−) and Ebi3^(−/−) Tregs, which are unable to secrete IL-10 and IL-35 respectively, were unable to suppress WT Tconv across a Transwell (FIG. 2C). Second, IL-10 and IL-35 neutralizing mAbs prevented Transwell suppression mediated by WT Tregs (FIG. 2D). Although Sema4a:Nrp1 ligation appeared to enhance Treg function, the inventors reasoned that it might also enhance Treg survival and/or stability in vitro. Indeed, Sema4a stimulation reduced the amount of cell death as determined by Annexin V and 7-AAD staining in an Nrp1-dependent manner (FIG. 2E). Subsequent qPCR analysis of wild-type and Nrp1-deficient Tregs cultured in the presence of isotype or Sema4a-Ig for 72 h with anti-CD3, anti-CD28, and IL-2 and intracellular cytokine staining for IL-10 of cells stimulated in the presence of isotype or Sema4a-Ig for 72 h with anti-CD3, anti-CD28, and IL-2 (Brefeldin A added for the last 8 hours of stimulation) revealed that IL-10 mRNA levels were not increased by Sema4a-Nrp1 ligation and the percentage of IL-10⁺ Tregs by ICS was not increased. Nevertheless, as determined by IL-10 ELISA and IL-35 IP/IB from supernatants of cells, both IL-10 and IL-35 were elevated in cultures when wild type but not Nrp1-deficient Tregs were stimulated with anti-CD3, anti-CD28 and Sema4a-Ig. Taken together, these data suggest that Nrp1 ligation by Sema4a potentiates IL-10/IL-35-dependent suppression and enhanced Treg survival and longevity in vitro.

Although it has been suggested that NRP1 is not expressed on human Tregs²⁵, this has not been rigorously assessed on activated or functionally suppressive Tregs. As human Tregs can require activation in order to gain maximal suppressive function^(12,26), the present inventors reasoned that NRP1 may only be expressed on functionally suppressive Tregs. Consistent with previous studies²⁵, resting umbilical cord blood Tregs and Tconv cells did not express NRP1 (FIG. 2F). Although activation with anti-CD3, anti-CD28 and IL-2 induced early NRP1 expression by both T cell populations, Tregs exhibited long-term stable expression of NRP1. It was then assessed whether an NRP1-SEMA4A axis could potentiate human Treg function. As previously shown²⁶, Tconv can potentiate human Treg suppression across a permeable Transwell membrane (FIG. 2G). Importantly, this suppressive activity was blocked by anti-NRP1 mAbs, while immobilized human SEMA4A was sufficient to potentiate human Treg function in the absence of Tconv (FIG. 2G). These data support the possibility that the same pathway is active in murine and human Tregs.

Nrp1-Deficient Tregs Maintain Immune Homeostasis

Given that disruption of the Nrp1:Sema4a axis diminishes Treg activity in vitro, the present inventors posited that Treg function might be compromised in vivo, particularly at highly inflammatory sites. Foxp3-deficient mice develop a strong autoimmune condition, reminiscent of the human disease IPEX. This is characterized my massive immune infiltration and tissue inflammation which is lethal by 3-6 weeks^(2,27). Thus disruption of Treg function in vivo could lead to the development of an inflammatory disease. Nrp1^(f/f)Foxp3^(Cre) mice and their age- and sex-matched littermate Foxp3^(Cre) controls were observed for 10 months and a detailed histological analysis of all organs typically targeted in Treg-deficient mice was performed. Blinded analysis demonstrated that Nrp1^(f/f)Foxp3^(Cre) mice were within normal limits in all respects including outward appearance, and histological analysis of skin, lung, liver, intestines, pancreas, kidney, salivary glands and spleen. No alterations in the size, percentage or phenotype of T cell subpopulations, as determined by flow cytometric analysis, were observed. Thus, no alteration in immune homeostasis, development of inflammatory disease or autoimmunity could be detected in aged mice with a restricted deletion of Nrp1 on Tregs.

The autoimmune phenotype of Foxp3-deficient mice can be substantially delayed by the adoptive transfer of Tregs into 2 day old mice, which can persist for several months before the mice succumb to the disease^(2,27). Disease onset, prevalence, clinical and histological scores (of liver, lung, and ear pinna) were all identical between Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) Treg recipients (FIG. 3). Collectively, these data indicate that expression of Nrp1 on Tregs is dispensable for the maintenance of immune homeostasis and the prevention of inflammatory and autoimmune disease that would normally develop in the absence of Tregs.

Nrp1-Deficient Tregs Fail in Inflammatory Environments

Tregs represent a major barrier to effective anti-tumor immunity in many cancers^(28,29). Treg depletion, via anti-CD25 treatment or use of Foxp3^(DTR-gfp) mice (in which Foxp3⁺ Treg express the diphtheria toxin receptor, allowing for their conditional depletion by DT administration), has been shown to greatly enhance anti-tumor immunity^(30,31). However, depletion of Tregs also results in massive lymphoproliferation and autoimmune disease similar to that seen in Foxp3-deficient mice³². As tumors represent a highly inflammatory environment, the capacity of Nrp1-deficient Tregs to mediate tumor-induced tolerance and prevent effective anti-tumor immunity was assessed. Three transplantable tumor models were used: MC38 (an immunogenic colon carcinoma line), EL4 (a moderately immunogenic thymoma), and B16 (a poorly immunogenic melanoma)^(33,34). Although complete Treg loss by DT treatment of tumor-inoculated Foxp3^(DTR-gfp) mice resulted in tumor clearance, mice succumb to autoimmune-mediated lethality around three weeks post-DT treatment (FIG. 4A-C).

Tumor growth in Nrp1^(f/f)Foxp3^(Cre) mice and their Foxp3^(Cre) littermate controls was then assessed. Significantly delayed MC38 tumor growth was observed in Nrp1^(f/f)Foxp3^(Cre) mice, despite the absence of any complete remission (CR) (FIG. 4A). In contrast, CR was observed in ˜40% of EL4-inoculated Nrp1^(f/f)Foxp3^(Cre) mice with greatly reduced tumor growth in almost all mice (FIG. 4B). Strikingly, CR was observed in two-thirds of the B16-inoculated Nrp1^(f/f)Foxp3^(Cre) mice, with reduced tumor growth in the remaining mice (FIG. 4C). Using a lung metastatic B16 model, Foxp3^(Cre) animals developed a dose-dependent increase in the number of metastases while Nrp1^(f/f)Foxp3^(Cre) mice exhibited almost complete clearance, even at high tumor doses (FIG. 4D). Analysis of B16 tumor-infiltrating lymphocytes (TILs) in the skin showed that while both Treg populations can infiltrate tumors, Nrp1-deficient Tregs have a limited ability to suppress effector CD8⁺ T cell proliferation and cytokine production, particularly in the highly tumoricidal IFNγ⁺TNFα⁺IL-2⁺ subset (FIG. 4E)³⁵. Thus, the program driven by Nrp1 signaling in Tregs is critically important for suppressing anti-tumor immunity.

The present inventors also sought to determine what cells expressed Sema4a in the tumor microenvironment. Surprisingly, conventional DCs (cDCs), CD8⁺ T_(conv) cells, NK cells, and to a lesser degree CD4⁺ T_(conv) cells downregulate Sema4a surface expression in the TIL compared to the draining and nondraining lymph nodes (FIG. 4H). Instead, the majority of Sema4a^(hi) tumor-infiltrating cells (˜57%) were PDCA1⁺B220⁺CD11c⁺ plasmacytoid dendritic cells (pDCs) (FIG. 4H). While surprising, this finding was consistent with previous literature suggesting that pDCs can be tolerogenic, and that depletion of pDCs resulted in increased antitumor immunity (Demoulin et al., J Leukoc Biol 93, 343-352 (2013); Faget et al., Cancer Res 72, 6130-6141 (2012); Sawant et al., J Immunol 189, 4258-4265, (2012)). Indeed, in Transwell suppression assays using Treg cocultured with pDCs sorted from spleen and lymph node preparations, activated overnight with CpG oligonucleotides, and fixed briefly in 1% PFA followed by extensive washing, pDCs could potentiate T_(reg) function in Transwell suppression assays in a Sema4a-dependent manner.

Previous studies have shown the Nrp1 domains that bind semaphorins are district from those that bind VEGF⁴⁰. In order to provide further support for a Sema4a-Nrp1 axis mediating T_(reg)-induced tumor tolerance, the present inventors utilized Sema4a and Nrp1-specific mAbs that disrupt Nrp1-Sema4a but not Nrp1-VEGF interaction. Specifically, ELISA-based binding assays were performed using plates coated with 500 ng/mL recombinant mNrp1 incubated with either (i) anti-Nrp1 or mouse IgG1 in the presence of 50 ng/mL VEGF165 (detected using anti-VEGF biotin) or (ii) Sema4a-Ig or mouse IgG1, in the presence of isotype controls, anti-Nrp1, or anti-Sema4a (Sema4a-Ig or mouse IgG1 were detected using an anti-isotype antibody). Wild-type C57/BL6 mice inoculated with B16 melanoma and given twice-weekly injections of Nrp1 or Sema4a blocking mAbs (100 μg; R&D Systems, clone 757129) exhibited significantly reduced tumor growth compared to those given isotype control (FIG. 4I). Importantly, the effect of the Nrp1 and Sema4a blocking mAbs was essentially identical. Furthermore, utilization of Sema4a-Ig as a soluble antagonist in vivo also resulted in significantly reduced tumor growth (FIG. 4J), associated with similar increases in CD8⁺ T cell tumor infiltration. To determine whether Nrp1 blockade could have therapeutic utility, B16 tumor-bearing C57/BL6 mice were treated with higher doses (400 μg initial dose, 200 μg twice weekly) of Nrp1 blocking mAb. Remarkably, tumor growth was reduced with this single modality treatment, with CR in some mice (FIG. 4F).

Nrp1-dependent Treg function could also be broadly important in suppressing responses in other established, highly inflammatory environments. Adoptive transfer of naïve CD4⁺CD45RB^(hi) Tconv cells into Rag1^(−/−) mice induces highly inflammatory colitis, similar to human inflammatory bowel disease (IBD), that can be rescued by subsequent transfer of purified Tregs^(13,36). Indeed, injection of Tconv cells into Rag1^(−/−) mice resulted in significant weight loss and immune pathology, which could be rescued by Foxp3^(Cre) Treg (FIG. 4G). However, Nrp1-deficient Tregs failed to ameliorate colitis, resulting in significant weight loss and immune pathology. Thus, Nrp1-mediated Treg function is required for curing an established inflammatory disease, such as colitis.

Nrp1 Ligation Restrains Akt-mTOR Via PTEN to Initiate Foxo-Mediated Treg Stabilization

Although signaling downstream of Nrp1 in tumor lines, neurons and endothelium has been studied following ligation by VEGF or class III semaphorins^(15,17), the Nrp1 signaling pathway induced by a class IV semaphorins in Tregs has been unknown. Interestingly, Nrp1 has been shown to modulate Akt (protein kinase B) activity in some systems^(37,38). As Akt-mTOR activity has been shown to be detrimental to Treg function^(39,40), the present inventors hypothesized that Nrp1 ligation might inhibit Akt activation. Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) Tregs were stimulated in the presence of Sema4a-Ig- or IgG-coated beads and Akt-mTOR activation assessed by flow cytometry. Nrp1 ligation limited phosphorylation of Akt S473 as well as phosphorylation of S6K1 T389 in Tregs, which are required for its activation (FIG. 5A). Akt phosphorylation was also examined at the immunologic synapse (IS) using total internal reflection fluorescent (TIRF) microscopy. Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) Tregs were stimulated with a lipid bilayer containing anti-TCR mAb and either Sema4a-Ig or an IgG isotype control. Robust recruitment of Nrp1 to the IS was observed when Sema4a was present which coincided with an Nrp1-dependent loss of Akt activity despite equivalent global phosphotyrosine staining at the IS (FIGS. 5B and 6A-B).

To determine whether Akt inactivation was sufficient for Treg potentiation, Tregs were transduced with retrovirus encoding either wild-type (WT) or dominant negative kinase-dead (DN) Akt. Tregs transduced with DN, but not WT, Akt could mediate Transwell suppression to an extent comparable to that induced by Sema4a-Ig, suggesting that repressed Akt-mTOR activity downstream of Nrp1 is the dominant pathway driving Treg potentiation.

Nrp1 has a small cytoplasmic domain with a C-terminal PDZ domain-binding motif (amino acid sequence: SEA) (Pellet-Many et al., Biochem J 411, 211-226 (2008)). The present inventors hypothesized that this domain is required for Sema4a-dependent loss of pAkt at the IS. Neuropilin-deficient Tregs were transduced with retrovirus encoding WT Nrp1 or a PDZ domain binding motif-deficient Nrp1 mutant. Interestingly, loss of the PDZ domain binding motif completely abrogated the ability of Nrp1 to inhibit Akt activation at the IS following Sema4a ligation (Fig.), suggesting that this motif is recruiting a molecular inhibitor of Akt signaling.

Phosphatase and tensin homolog (PTEN) has been shown to inhibit Akt activation⁴¹. While PTEN appears to be dispensable for contact-dependent Treg suppression⁴², the present inventors hypothesized that PTEN may contribute to Nrp1-mediated inactivation of Akt. Low level, constitutive PTEN association with Nrp1 was observed in resting and activated Tregs, which was substantially enhanced by Sema4a ligation (FIG. 5C). In addition, PTEN-deficient Treg were unable to mediate Tconv and Sema4a-Ig induced Transwell suppression (FIG. 5D). Lastly, PTEN-deficient Tregs failed to inhibit Akt activation at the IS despite robust Nrp1 recruitment by Sema4a (as determined by TIRF microscopy of IS recruitment of neuropilin and activation of Akt in Foxp3^(Cre) or Pten^(f/f)Foxp3^(Cre) Treg purified flow cytometrically and then stimulated for 20 minutes on a lipid bilayer containing anti-TCR and either IgG or Sema4a-Ig; see FIG. 6C-D). These data suggest that PTEN is required for Nrp1-mediated repression of Akt activation at the IS and Treg functional potentiation.

Akt activity can hamper the Treg suppressive program in part by regulating the nuclear localization of Foxo transcription factor family members, as Akt-mediated phosphorylation promotes their nuclear exclusion via 14-3-3 binding⁴³⁻⁴⁵. Foxos play a key role in controlling Treg development and function by regulating Foxp3 expression, promoting a cohort of Treg-associated genes and limiting the expression of T cell-lineage specific transcription factors and effector molecules. As expected, unstimulated Treg show nuclear Foxo staining, while activated Treg exclude Foxo from the nucleus. In contrast, inclusion of Sema4a-Ig inhibited Foxo nuclear exclusion.

To determine the transcriptional program that promotes Nrp1-mediated Treg potentiation, gene expression profiling was conducted on Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) Tregs stimulated in the presence of Sema4a-Ig- or IgG1-coated beads in vitro. Specifically, Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) CD45Rb^(lo) Foxp3 (YFP)⁺ CD4⁺ T cells were stimulated for 48 hours with anti-CD3, anti-CD28, 100 U/mL rhIL-2, and immobilized IgG1 or Sema4a-Ig. RNA extracted from these cells was subjected to Affymetrix gene profiling analysis. Microarray data was then subjected to Gene Set Enrichment Analysis (GSEA) analysis using MSigDB providing enrichment score (ES), normalized enrichment score (NES) and False Discovery Rate (FDR) for given gene sets. Also, Gene Ontology DAVID analysis was performed for genes affected by Sema4a in Foxp3^(Cre) Treg but not Nrp1^(f/f) Foxp3^(Cre) Treg.

In general, the transcriptional changes associated with Nrp1 ligation in Tregs are consistent with enhanced phenotypic stability. Gene Set Enrichment Analysis (GSEA) and DAVID Gene Ontology analysis revealed several pathways upregulated by Sema4a ligation, including T cell homeostasis and IL-7 signaling, IL-2 downregulated genes, CD28 reactive genes, genes related to T cell differentiation, and several gene sets associated with disease phenotypes (Tables 1 and 3). Statistical analysis of the most upregulated genes revealed those associated with homeostasis, especially the Foxo target Klf2⁴⁶, as well as several transcription factors, cell surface molecules, and the anti-apoptotic Bcl2 (Table 3). In addition, by comparing gene expression profiles from freshly isolated T_(conv) and T_(regs) from Foxp3^(Cre) mice, an internally-controlled T_(reg) signature was obtained which was consistent with those previously reported⁵. Several T_(reg) signature genes were upregulated, including Helios (Ikzf2), Gpr83, Nt5e and Socs2. A subset was confirmed by qPCR (Ikzf2, Socs2, Bcl2, Nt5e, Klf2, Gpr83) and flow cytometry (KLF2, Helios, Bcl2, CD62L, CD127, CD73).

Interestingly, Nrp1 signaling induces the downregulation of several T cell lineage-specific transcription factors (Irf4, Rorg, Eomes) and their targets (Il4, Il5, Il17a) (Table 3). In addition, some regulators of cell signaling (Nedd4, Rgs16, Serpine2) and the checkpoint inhibitor Lag3 were also downregulated. The downregulation of Irf4, Irf8, Rorc, and Rgs16 was confirmed by qPCR. Overall, the transcriptional profile induced by Nrp1 signaling may promote Treg stability, quiescence and survival, while inhibiting programs that would drive or promote Treg terminal differentiation. It is also notable that there appears to be considerable overlap between the transcriptional program mediated by Nrp1 and the Foxos⁴⁵.

Foxo proteins can promote the transcription of several genes, which were also upregulated by Sema4a stimulation (Table 3)^(45,47). A gene of particular interest is Klf2, which was upregulated in response to Nrp1 and promotes expression of genes associated with T cell survival, longevity and memory, such as CD62L (Sell) and CD127/IL-7Rα (Il7ra)⁴⁷. Indeed, Treg stimulation in the presence of Sema4a limited their activation-induced downregulation suggesting that the Foxo/KLF2 axis is active in Treg stimulated via Nrp1.

Nrp1 signaling also induces the downregulation of several gene subsets defined by GSEA, including IRF4 targets, cytokine transcripts (114, 115, Ill 7a), Foxp3 downregulated genes, and IL-2 upregulated genes, among others (Table 2). Target genes validated by qPCR or protein analysis include several T cell lineage-specific transcription factors (Irf4, Rorc, Eomes), regulators of cell signaling (Rgs16) and the inhibitory receptor Lag3. Overall, the transcriptional profile induced by Nrp1 signaling may promote T_(reg) stability, quiescence and survival, while inhibiting programs that would drive or promote T_(reg) terminal differentiation and apoptosis.

In order to determine if the signaling and transcriptional events observed in vitro were physiologically relevant, key observations were assessed in tumor-infiltrating Tregs. However, it should be noted that only a subset of Nrp1^(f/f)Foxp3^(Cre) mice develop tumors following B16 injection and thus the tumors sampled would represent those where the consequence of Nrp1 loss on Tregs was less substantive. First, non-draining lymph nodes and TIL were harvested from tumor-bearing Foxp3^(Cre) and Nrp1^(f/f)Foxp3^(Cre) mice and assayed for Akt activation ex vivo. Whereas non-draining LN showed relatively high Akt activation in Treg, tumor-infiltrating Foxp3^(Cre) Treg displayed lower Akt activation (FIG. 7A). Importantly, the modulation of Akt activity in the tumor microenvironment was lost in Nrp1^(f/f)Foxp3^(Cre) Tregs supporting Nrp1-driven modulation of Tregs in vivo. Second, protein targets of Nrp1 signaling in TIL were examined, compared to other lymphoid compartments, and found that Helios was upregulated intratumor Tregs, while IRF4 and RORγt were downregulated in vivo in an Nrp1-dependent manner (FIG. 7B-C). Thirdly, this Nrp1-driven program resulted in increased intra-tumoral Treg proliferation and reduced apoptosis, as assessed by Ki67 expression and BrdU incorporation (FIG. 7E), and enhanced cleaved caspase 3 staining (FIG. 7D-E). The enhanced Nrp1-dependent T_(reg) survival observed correlated with enhanced expression of the anti-apoptotic factor Bcl2 (FIG. 7F). Finally, the impact of these changes on intratumoral T_(reg) suppressive mechanisms was examined. Although mRNA levels of IL-10 were not altered, there was an Nrp1-dependent enhancement of intratumoral IL-10⁺ T_(regs) (FIG. 7G). Furthermore, there was also an Nrp1-dependent maintenance of the extracellular adenosine producing molecule CD73 and the checkpoint inhibitor LAG-3 (FIG. 7H). Thus, Nrp1 signaling provides a critical switch that enforces Treg stability in inflammatory environments.

DISCUSSION

The data provided herein demonstrate that cell contact-dependent potentiation of Treg function is mediated via Sema4a-mediated Nrp1 ligation via a PTEN:Akt:Foxo axis (FIG. 8). Notably, Nrp1 appears to be one of a limited number of cell surface receptors (e.g., PD-148 and CTLA-449) that has been suggested to limit Akt activity in T cells. While Nrp1 under certain circumstances can modulate or even activate Akt signaling (Banerjee et al., Biochemistry 47, 3345-3351 (2008); Cao et al., Cancer Res 68, 8667-8672 (2008); Fukasawa et al., Cancer Biol Ther 6, 1173-1180 (2007); Kim et al., J Immunol 177, 5727-5735 (2006)), the specific context in which Nrp1 functions in T_(regs) (e.g., recruitment to the IS, unique cell type, transmembrane vs soluble ligand) may provide a distinct environment that facilitates PTEN recruitment and loss of Akt activity. This pathway enhances Treg function indirectly by enforcing stability and promoting survival, which is most evident in inflammatory sites such as in tumors and colitic intestinal mucosa. The issue of Treg stability/plasticity has been highly contentious, and the cell-extrinsic stimuli and mechanisms which maintain Treg stability remain elusive⁸⁻¹¹. Given that Foxo family members enhance Foxp3 function and promote Treg homeostasis and function⁴⁵, it is noteworthy that Nrp1 signaling counteracts the negative impact of Akt on Foxo nuclear localization. Indeed, there is substantial overlap between the transcriptional profiles induced by Foxo and Nrp1 signaling⁴⁵. It is also interesting that Nrp1 signaling modulates the expression of several KLFs (Klf2, Klf1), which are known to be involved in cell quiescence⁴⁶. A transcription factor quintet has also recently been shown to ‘lock-in’ the Treg transcriptional signature⁴. Interestingly, some of these transcription factors are modulated by Nrp1 signaling (e.g., Ikzf2, Irf4, Gata1), suggesting that Sema4a-mediated Nrp1 ligation may constitute a cell-extrinsic regulator of this program. Collectively, the observations provided herein suggest that the Sema4a:Nrp1 axis is required to maintain Treg stability at inflammatory sites. Furthermore, it is possible that the Nrp1:Sema4a pathway may be perturbed under certain pathological or genetic circumstances which could also provide a basis for the seemingly contradictory perceptions of Treg stability versus plasticity in a variety of normal and diseased states. Given that memory CD4⁺ and CD8⁺ T cells have been shown to express Nrp1, it is possible that restrained Akt-mTOR activation may facilitate maintainance of the memory T cell phenotype (Powell et al., Annu Rev Immunol 30, 39-68 (2012)).

As Tregs represent a major barrier to effective anti-tumor immunity in many cancers^(28,29), a prevailing question of clinical importance is whether it is possible to limit Treg function in tumors while preventing inflammatory or autoimmune adverse events. It is also intriguing that a dominant source of Sema4a in the tumor studies described herein was the plasmacytoid DC. The present identification of the Nrp1:Sema4a axis as a pivotal pathway required for Treg stability at tumoral inflammatory sites but not for peripheral homeostatic maintenance suggests, for the first time, that Sema4a:Nrp1 blockade via antibodies or soluble antagonists might be a viable therapeutic strategy to limit tumor-induced tolerance without evoking autoimmunity.

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The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description. Such modifications are intended to fall within the scope of the appended claims.

All patents, applications, publications, test methods, literature, and other materials cited herein are hereby incorporated by reference in their entirety as if physically present in this specification.

TABLE 1 NOM p- FDR q- FWER p- RANK NAME SIZE ES NES val val val AT MAX LEADING EDGE MOSERLE_IFNA_RESPONSE 20 0.780182 2.287744 0 0 0 3771 tags = 80%, list = 17%, signal = 97% BASSO_CD40_SIGNALING_DN 57 0.582034 2.177623 0 0.001544 0.005 4626 tags = 54%, list = 21%, signal = 69% TAKEDA_TARGETS_OF_NUP98_(—) 123 0.503057 2.161499 0 0.001646 0.008 4687 tags = 45%, HOXA9_FUSION_3D_UP list = 21%, signal = 57% ZHAN_V1_LATE_DIFFERENTIATION_(—) 29 0.604006 1.993054 0 0.027944 0.163 2268 tags = 34%, GENES_UP list = 10%, signal = 38% BOYLAN_MULTIPLE_MYELOMA_(—) 92 0.483428 1.95568 0 0.039941 0.275 2885 tags = 37%, PCA1_UP list = 13%, signal = 42% MORI_PRE_BI_LYMPHOCYTE_DN 59 0.514033 1.948411 0 0.035463 0.29 5476 tags = 49%, list = 25%, signal = 65% BENNETT_SYSTEMIC_LUPUS_(—) 15 0.708549 1.943889 0 0.032521 0.309 1214 tags = 40%, ERYTHEMATOSUS list = 6%, signal = 42% DIAZ_CHRONIC_MEYLOGENOUS_(—) 93 0.46659 1.927104 0 0.036564 0.377 4481 tags = 40%, LEUKEMIA_DN list = 20%, signal = 50% VALK_AML_CLUSTER_13 23 0.601074 1.888098 0 0.05322 0.546 2951 tags = 30%, list = 13%, signal = 35% LEE_DIFFERENTIATING_T_(—) 108 0.453179 1.885657 0 0.049074 0.553 6782 tags = 53%, LYMPHOCYTE list = 31%, signal = 76% SHIPP_DLBCL_VS_FOLLICULAR_(—) 37 0.531142 1.841607 0.001667 0.078602 0.748 3348 tags = 41%, LYMPHOMA_DN list = 15%, signal = 48% KOBAYASHI_EGFR_SIGNALING_(—) 74 0.468195 1.834232 0 0.078615 0.774 6106 tags = 55%, 24HR_UP list = 28%, signal = 77% TAKEDA_TARGETS_OF_NUP98_(—) 116 0.431239 1.832117 0 0.074563 0.783 3846 tags = 34%, HOXA9_FUSION_8D_UP list = 18%, signal = 41% KIM_LRRC3B_TARGETS 17 0.646053 1.821081 0.001905 0.077972 0.824 2963 tags = 41%, list = 14%, signal = 48% FARMER_BREAST_CANCER_(—) 30 0.552833 1.813877 0.001718 0.079269 0.844 3680 tags = 43%, CLUSTER_1 list = 17%, signal = 52% BROWNE_INTERFERON_RESPONSIVE_(—) 51 0.485545 1.804869 0 0.081404 0.867 4417 tags = 43%, GENES list = 20%, signal = 54% LIAN_LIPA_TARGETS_6M 78 0.448416 1.799782 0.00159 0.081092 0.885 2866 tags = 37%, list = 13%, signal = 43% FLECHNER_BIOPSY_KIDNEY_(—) 76 0.448979 1.798828 0 0.077551 0.889 5328 tags = 43%, TRANSPLANT_REJECTED_VS_OK_UP list = 24%, signal = 57% EINAV_INTERFERON_SIGNATURE_(—) 18 0.610528 1.781675 0.003617 0.08978 0.927 5629 tags = 61%, IN_CANCER list = 26%, signal = 82% YU_MYC_TARGETS_DN 53 0.478017 1.767861 0.001698 0.098859 0.952 5167 tags = 47%, list = 24%, signal = 62% BOYLAN_MULTIPLE_MYELOMA_(—) 247 0.37653 1.761921 0 0.100015 0.96 4439 tags = 36%, C_D_DN list = 20%, signal = 45% RODRIGUES_DCC_TARGETS_DN 105 0.420315 1.75343 0 0.103495 0.971 2763 tags = 28%, list = 13%, signal = 31% ZHANG_INTERFERON_RESPONSE 15 0.639616 1.753212 0.003697 0.099156 0.971 3609 tags = 47%, list = 16%, signal = 56% ZHAN_MULTIPLE_MYELOMA_(—) 35 0.51926 1.7504 0.001757 0.097936 0.973 3855 tags = 49%, PR_DN list = 18%, signal = 59% ODONNELL_TARGETS_OF_(—) 54 0.467824 1.749903 0.001757 0.094416 0.973 5445 tags = 54%, MYC_AND_TFRC_UP list = 25%, signal = 71% WIELAND_UP_BY_HBV_INFECTION 75 0.438772 1.740891 0 0.099804 0.979 2632 tags = 24%, list = 12%, signal = 27% LIU_VAV3_PROSTATE_(—) 78 0.435901 1.721277 0 0.117502 0.994 6060 tags = 50%, CARCINOGENESIS_UP list = 28%, signal = 69% MORI_MATURE_B_(—) 72 0.439127 1.718323 0.001658 0.116508 0.995 4855 tags = 38%, LYMPHOCYTE_UP list = 22%, signal = 48% DAUER_STAT3_TARGETS_DN 28 0.536905 1.715527 0.00726 0.11592 0.996 4417 tags = 57%, list = 20%, signal = 71% HOFFMANN_IMMATURE_TO_(—) 26 0.540776 1.714734 0.009259 0.113128 0.996 1683 tags = 31%, MATURE_B_LYMPHOCYTE_ UP list = 8%, signal = 33% ICHIBA_GRAFT_VERSUS_HOST_(—) 105 0.410042 1.713352 0 0.111118 0.996 6418 tags = 48%, DISEASE_D7_UP list = 29%, signal = 67% TAKEDA_TARGETS_OF_NUP98_(—) 133 0.385752 1.691537 0 0.133156 0.999 4645 tags = 36%, HOXA9_FUSION_10D_UP list = 21%, signal = 46% ZIRN_TRETINOIN_RESPONSE_(—) 17 0.591184 1.689255 0.013283 0.132356 1 5401 tags = 59%, WT1_UP list = 25%, signal = 78% MCCABE_HOXC6_TARGETS_DN 17 0.586301 1.683937 0.010772 0.13554 1 3036 tags = 35%, list = 14%, signal = 41% YAO_TEMPORAL_RESPONSE_TO_(—) 16 0.58783 1.675209 0.009191 0.143467 1 1698 tags = 25%, PROGESTERONE_CLUSTER_3 list = 8%, signal = 27% WIKMAN_ASBESTOS_LUNG_CANCER_(—) 22 0.535219 1.668022 0.024074 0.149581 1 2001 tags = 32%, DN list = 9%, signal = 35% WINTER_HYPOXIA_DN 40 0.472244 1.664049 0 0.150173 1 4581 tags = 48%, list = 21%, signal = 60% SMID_BREAST_CANCER_NORMAL_(—) 362 0.3405 1.6616 0 0.149654 1 4626 tags = 33%, LIKE_UP list = 21%, signal = 42% LIAN_LIPA_TARGETS_3M 65 0.434176 1.661359 0.001672 0.146133 1 3112 tags = 35%, list = 14%, signal = 41% CAIRO_HEPATOBLASTOMA_(—) 172 0.367863 1.659135 0 0.145556 1 5734 tags = 37%, CLASSES_DN list = 26%, signal = 50% ROSS_AML_WITH_CBFB_(—) 43 0.464084 1.658638 0.003559 0.142786 1 5542 tags = 51%, MYH11_FUSION list = 25%, signal = 68% YAO_TEMPORAL_RESPONSE_TO_(—) 71 0.417113 1.646051 0 0.15584 1 5708 tags = 52%, PROGESTERONE_CLUSTER_0 list = 26%, signal = 70% HADDAD_T_LYMPHOCYTE_AND_(—) 55 0.436019 1.64187 0.00659 0.1582 1 1281 tags = 25%, NK_PROGENITOR_DN list = 6%, signal = 27% HESS_TARGETS_OF_HOXA9_(—) 76 0.41417 1.631702 0.007874 0.169431 1 5960 tags = 51%, AND_MEIS1_DN list = 27%, signal = 70% DUNNE_TARGETS_OF_AML1_(—) 36 0.478438 1.629428 0.010582 0.168833 1 2167 tags = 28%, MTG8_FUSION_UP list = 10%, signal = 31% YAO_TEMPORAL_RESPONSE_(—) 71 0.409811 1.621562 0.001692 0.176764 1 5217 tags = 38%, TO_PROGESTERONE_CLUSTER_1 list = 24%, signal = 50% ST_ADRENERGIC 31 0.488004 1.61073 0.019097 0.190594 1 4284 tags = 29%, list = 20%, signal = 36% RAMALHO_STEMNESS_DN 69 0.409625 1.609626 0.007092 0.188375 1 5444 tags = 36%, list = 25%, signal = 48% YANG_BREAST_CANCER_(—) 15 0.570111 1.608223 0.022642 0.186854 1 4987 tags = 33%, ESR1_BULK_UP list = 23%, signal = 43% GUTIERREZ_CHRONIC_LYMPHOCYTIC_(—) 46 0.444619 1.606409 0.014363 0.185868 1 4049 tags = 35%, LEUKEMIA_DN list = 18%, signal = 43% MARKEY_RB1_ACUTE_LOF_UP 215 0.342148 1.601109 0 0.1904 1 6081 tags = 40%, list = 28%, signal = 55% REACTOME_CD28_CO_(—) 25 0.509357 1.592281 0.014519 0.201624 1 4052 tags = 28%, STIMULATION list = 19%, signal = 34% SEITZ_NEOPLASTIC_TRANSFORMATION_(—) 60 0.417038 1.581352 0.011419 0.216585 1 5045 tags = 42%, BY_8P_DELETION_UP list = 23%, signal = 54% RIZ_ERYTHROID_DIFFERENTIATION_12HR 41 0.447639 1.580376 0.017575 0.214328 1 4839 tags = 32%, list = 22%, signal = 41% CHUNG_BLISTER_CYTOTOXICITY_DN 28 0.484896 1.579003 0.016129 0.212803 1 4644 tags = 46%, list = 21%, signal = 59% YANG_BREAST_CANCER_ESR1_UP 19 0.540089 1.575191 0.024528 0.215073 1 4051 tags = 37%, list = 19%, signal = 45% FULCHER_INFLAMMATORY_RESPONSE_(—) 318 0.326276 1.568222 0 0.223651 1 5907 tags = 36%, LECTIN_VS_LPS_DN list = 27%, signal = 49% ZUCCHI_METASTASIS_UP 20 0.531876 1.565082 0.023636 0.22572 1 3847 tags = 30%, list = 18%, signal = 36% CHARAFE_BREAST_CANCER_ BASAL_VS_(—) 39 0.452651 1.563495 0.015652 0.224905 1 1668 tags = 23%, MESENCHYMAL_DN list = 8%, signal = 25% ZHAN_MULTIPLE_MYELOMA_DN 25 0.496399 1.556541 0.022887 0.234662 1 2712 tags = 28%, list = 12%, signal = 32% WEST_ADRENOCORTICAL_CARCINOMA_(—) 17 0.551168 1.548203 0.025194 0.246394 1 2788 tags = 29%, VS_ADENOMA_DN list = 13%, signal = 34% LIANG_HEMATOPOIESIS_STEM_ CELL_(—) 30 0.477597 1.547156 0.021016 0.244334 1 5927 tags = 43%, NUMBER_SMALL_VS_HUGE_DN list = 27%, signal = 59% NEWMAN_ERCC6_TARGETS_UP 19 0.514551 1.546377 0.032143 0.242099 1 3307 tags = 47%, list = 15%, signal = 56% TAKEDA_TARGETS_OF_NUP98_ HOXA9_(—) 124 0.363496 1.544956 0.003257 0.240995 1 3846 tags = 30%, FUSION_16D_UP list = 18%, signal = 36% GARGALOVIC_RESPONSE_TO_OXIDIZED_(—) 17 0.547073 1.537267 0.033028 0.252503 1 2897 tags = 29%, PHOSPHOLIPIDS_RED_DN list = 13%, signal = 34% ZHANG_ANTIVIRAL_RESPONSE_(—) 22 0.511479 1.536626 0.028725 0.249823 1 2272 tags = 27%, TO_RIBAVIRIN_UP list = 10%, signal = 30% ICHIBA_GRAFT_VERSUS_HOST_(—) 128 0.353342 1.533823 0.004992 0.25164 1 3262 tags = 25%, DISEASE_35D_UP list = 15%, signal = 29% XU_GH1_EXOGENOUS_TARGETS_DN 71 0.387572 1.527815 0.010017 0.259812 1 5208 tags = 41%, list = 24%, signal = 53% NAKAJIMA_MAST_CELL 28 0.475146 1.527363 0.036649 0.256969 1 1422 tags = 25%, list = 6%, signal = 27% RADAEVA_RESPONSE_TO_IFNA1_UP 28 0.475943 1.525465 0.025 0.257156 1 1652 tags = 21%, list = 8%, signal = 23% TAKEDA_TARGETS_OF_NUP98_HOXA9_(—) 142 0.346459 1.525141 0.003145 0.254247 1 5601 tags = 39%, FUSION_8D_DN list = 26%, signal = 53% ROY_WOUND_BLOOD_VESSEL_UP 41 0.439538 1.520434 0.028881 0.260229 1 3701 tags = 32%, list = 17%, signal = 38% KRASNOSELSKAYA_ILF3_TARGETS_UP 22 0.4992 1.514133 0.02852 0.269079 1 1532 tags = 27%, list = 7%, signal = 29% BIOCARTA_IL7_PATHWAY 17 0.529018 1.513342 0.054104 0.266965 1 6967 tags = 59%, list = 32%, signal = 86% SEKI_INFLAMMATORY_RESPONSE_(—) 22 0.50008 1.513179 0.028829 0.263809 1 5462 tags = 50%, LPS_DN list = 25%, signal = 67% CHEOK_RESPONSE_TO_HD_MTX_UP 15 0.54034 1.505168 0.052533 0.276692 1 4411 tags = 60%, list = 20%, signal = 75% REACTOME_GENERATION_OF_(—) 20 0.503759 1.503832 0.046632 0.275974 1 7129 tags = 55%, SECOND_MESSENGER_MOLECULES list = 33%, signal = 81% LIANG_SILENCED_BY_METHYLATION_2 26 0.476262 1.498888 0.036269 0.283112 1 2867 tags = 31%, list = 13%, signal = 35% GNATENKO_PLATELET_SIGNATURE 28 0.452962 1.495195 0.038321 0.287571 1 1177 tags = 7%, list = 5%, signal = 8% WALLACE_PROSTATE_CANCER_RACE_UP 213 0.324127 1.487432 0.003017 0.301274 1 3262 tags = 25%, list = 15%, signal = 29%

TABLE 2 NOM FDR FWER RANK NAME SIZE ES NES p-val q-val p-val AT MAX LEADING EDGE MANALO_HYPOXIA_DN 233 −0.6248 −3.10267 0 0 0 5952 tags = 75%, list = 27%, signal = 102% SHEDDEN_LUNG_CANCER_POOR_SURVIVAL_A6 363 −0.5568 −2.90709 0 0 0 6869 tags = 67%, list = 31%, signal = 96% ROSTY_CERVICAL_CANCER_PROLIFERATION_CLUSTER 119 −0.63271 −2.88451 0 0 0 5413 tags = 68%, list = 25%, signal = 90% CAIRO_HEPATOBLASTOMA_CLASSES_UP 491 −0.52038 −2.80827 0 0 0 6692 tags = 62%, list = 31%, signal = 87% SOTIRIOU_BREAST_CANCER_GRADE_1_VS_3_UP 119 −0.61776 −2.79674 0 0 0 6027 tags = 73%, list = 28%, signal = 100% KOBAYASHI_EGFR_SIGNALING_24HR_DN 210 −0.56625 −2.76693 0 0 0 4922 tags = 61%, list = 22%, signal = 78% FOURNIER_ACINAR_DEVELOPMENT_LATE_2 234 −0.54704 −2.72639 0 0 0 6692 tags = 60%, list = 31%, signal = 86% BERENJENO_TRANSFORMED_BY_RHOA_UP 474 −0.50701 −2.724 0 0 0 6265 tags = 61%, list = 29%, signal = 83% WONG_EMBRYONIC_STEM_CELL_CORE 294 −0.52557 −2.72324 0 0 0 6153 tags = 58%, list = 28%, signal = 80% YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_(—) 94 −0.61381 −2.66053 0 0 0 5876 tags = 67%, list = 27%, CLUSTER_11 signal = 91% CROONQUIST_IL6_DEPRIVATION_DN 70 −0.63924 −2.65141 0 0 0 6153 tags = 80%, list = 28%, signal = 111% HOFFMANN_LARGE_TO_SMALL_PRE_BII_(—) 89 −0.60027 −2.58164 0 0 0 4901 tags = 64%, list = 22%, LYMPHOCYTE_UP signal = 82% U_MYC_TARGETS_UP 37 −0.71553 −2.55861 0 0 0 5413 tags = 89%, list = 25%, signal = 118% ODONNELL_TARGETS_OF_MYC_AND_TFRC_DN 33 −0.72466 −2.55781 0 0 0 5292 tags = 91%, list = 24%, signal = 120% WINNEPENNINCKX_MELANOMA_METASTASIS_UP 119 −0.56021 −2.55758 0 0 0 6951 tags = 73%, list = 32%, signal = 107% YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_(—) 115 −0.56693 −2.5469 0 0 0 7004 tags = 70%, list = 32%, CLUSTER_14 signal = 102% RODRIGUES_THYROID_CARCINOMA_POORLY_(—) 489 −0.46802 −2.53179 0 0 0 5968 tags = 51%, list = 27%, DIFFERENTIATED_UP signal = 68% FUJII_YBX1_TARGETS_DN 125 −0.54196 −2.49594 0 0 0 4939 tags = 53%, list = 23%, signal = 68% CROONQUIST_NRAS_SIGNALING_DN 54 −0.63419 −2.48885 0 0 0 6153 tags = 76%, list = 28%, signal = 105% GRAHAM_NORMAL_QUIESCENT_VS_NORMAL_DIVIDING_(—) 70 −0.60518 −2.48278 0 0 0 6063 tags = 76%, list = 28%, DN signal = 104% REACTOME_LATE_PHASE_OF_HIV_LIFE_CYCLE 87 −0.5748 −2.47952 0 0 0 8431 tags = 80%, list = 39%, signal = 130% KAUFFMANN_MELANOMA_RELAPSE_UP 54 −0.62378 −2.47485 0 0 0 5554 tags = 59%, list = 25%, signal = 79% SCHUHMACHER_MYC_TARGETS_UP 61 −0.61714 −2.471 0 0 0 5506 tags = 64%, list = 25%, signal = 85% REACTOME_CELL_CYCLE_MITOTIC 262 −0.48339 −2.46512 0 0 0 6909 tags = 56%, list = 32%, signal = 81% KAUFFMANN_DNA_REPAIR_GENES 187 −0.50159 −2.46045 0 0 0 6218 tags = 55%, list = 28%, signal = 76% PUJANA_BRCA_CENTERED_NETWORK 89 −0.56638 −2.45856 0 0 0 7277 tags = 73%, list = 33%, signal = 109% REACTOME_MITOTIC_M_M_G1_PHASES 135 −0.53123 −2.44983 0 0 0 6909 tags = 60%, list = 32%, signal = 87% REACTOME_SNRNP_ASSEMBLY 45 −0.65052 −2.44495 0 0 0 6439 tags = 76%, list = 29%, signal = 107% BASAKI_YBX1_TARGETS_UP 222 −0.49822 −2.44417 0 0 0 5554 tags = 57%, list = 25%, signal = 75% ODONNELL_TFRC_TARGETS_DN 97 −0.55664 −2.43787 0 0 0 6126 tags = 68%, list = 28%, signal = 94% FRASOR_RESPONSE_TO_SERM_OR_FULVESTRANT_DN 41 −0.65506 −2.42734 0 0 0 4941 tags = 66%, list = 23%, signal = 85% REACTOME_HIV_LIFE_CYCLE 100 −0.54912 −2.4228 0 0 0 5861 tags = 59%, list = 27%, signal = 80% MUELLER_PLURINET 259 −0.47566 −2.41338 0 0 0 6395 tags = 54%, list = 29%, signal = 75% PUJANA_XPRSS_INT_NETWORK 140 −0.51444 −2.40556 0 0 0 7526 tags = 65%, list = 34%, signal = 98% RUIZ_TNC_TARGETS_DN 119 −0.53597 −2.40153 0 0 0 4777 tags = 51%, list = 22%, signal = 65% REACTOME_DNA_REPAIR 94 −0.55297 −2.39978 0 0 0 5861 tags = 61%, list = 27%, signal = 82% REACTOME_S_PHASE 96 −0.54082 −2.37791 0 0 0 6833 tags = 60%, list = 31%, signal = 87% BIDUS_METASTASIS_UP 158 −0.51165 −2.37316 0 0 0 7136 tags = 63%, list = 33%, signal = 93% WHITEFORD_PEDIATRIC_CANCER_MARKERS 86 −0.54806 −2.36761 0 3.93E−05 0.001 7069 tags = 72%, list = 32%, signal = 106% REACTOME_G2_M_CHECKPOINTS 40 −0.63598 −2.36258 0 3.83E−05 0.001 5555 tags = 70%, list = 25%, signal = 94% REACTOME_METABOLISM_OF_RNA 87 −0.54929 −2.35909 0 3.74E−05 0.001 7211 tags = 69%, list = 33%, signal = 102% NAKAMURA_CANCER_MICROENVIRONMENT_DN 41 −0.63668 −2.35679 0 3.65E−05 0.001 3730 tags = 56%, list = 17%, signal = 67% BENPORATH_PROLIFERATION 116 −0.51614 −2.35319 0 3.56E−05 0.001 6389 tags = 59%, list = 29%, signal = 82% LINDGREN_BLADDER_CANCER_CLUSTER_3_UP 251 −0.46393 −2.34652 0 3.48E−05 0.001 6686 tags = 54%, list = 31%, signal = 77% WAKASUGI_HAVE_ZNF143_BINDING_SITES 53 −0.59959 −2.3417 0 3.40E−05 0.001 5772 tags = 68%, list = 26%, signal = 92% SCHLOSSER_MYC_TARGETS_REPRESSED_BY_SERUM 121 −0.51909 −2.34105 0 3.33E−05 0.001 6356 tags = 57%, list = 29%, signal = 80% REACTOME_SYNTHESIS_OF_DNA 83 −0.54736 −2.30879 0 1.32E−04 0.004 8423 tags = 77%, list = 38%, signal = 125% REACTOME_TRANSPORT_OF_MATURE_MRNA_DERIVED_(—) 49 −0.59175 −2.29609 0 1.30E−04 0.004 7817 tags = 78%, list = 36%, FROM_AN_INTRON_CONTAINING_TRANSCRIPT signal = 120% REACTOME_MITOTIC_PROMETAPHASE 71 −0.55579 −2.2958 0 1.27E−04 0.004 6280 tags = 59%, list = 29%, signal = 83% GRAHAM_CML_DIVIDING_VS_NORMAL_QUIESCENT_(—) 152 −0.48848 −2.29571 0 1.24E−04 0.004 6063 tags = 65%, list = 28%, UP signal = 89% REACTOME_HIV_INFECTION 175 −0.47404 −2.29196 0 1.22E−04 0.004 8431 tags = 68%, list = 39%, signal = 110% REACTOME_DNA_REPLICATION_PRE_INITIATION 72 −0.54465 −2.28201 0 1.20E−04 0.004 8423 tags = 76%, list = 38%, signal = 124% MARKEY_RB1_ACUTE_LOF_DN 213 −0.46076 −2.27719 0 1.17E−04 0.004 5479 tags = 51%, list = 25%, signal = 67% REN_BOUND_BY_E2F 46 −0.60126 −2.27011 0 1.15E−04 0.004 6811 tags = 78%, list = 31%, signal = 113% BLUM_RESPONSE_TO_SALIRASIB_DN 307 −0.43985 −2.26538 0 1.42E−04 0.005 6203 tags = 50%, list = 28%, signal = 69% GARCIA_TARGETS_OF_FLI1_AND_DAX1_DN 110 −0.50543 −2.26225 0 1.68E−04 0.006 4187 tags = 47%, list = 19%, signal = 58% REACTOME_RNA_POLYMERASE_II_TRANSCRIPTION 86 −0.52681 −2.26175 0 1.65E−04 0.006 9169 tags = 80%, list = 42%, signal = 138% HESS_TARGETS_OF_HOXA9_AND_MEIS1_UP 61 −0.56804 −2.2611 0 1.62E−04 0.006 6153 tags = 69%, list = 28%, signal = 96% REACTOME_CELL_CYCLE_CHECKPOINTS 105 −0.51244 −2.26088 0 1.59E−04 0.006 8446 tags = 72%, list = 39%, signal = 117% TOYOTA_TARGETS_OF_MIR34B_AND_MIR34C 302 −0.43657 −2.25848 0 1.83E−04 0.007 5294 tags = 47%, list = 24%, signal = 62% LE_EGR2_TARGETS_UP 99 −0.50456 −2.24365 0 2.57E−04 0.01 5571 tags = 60%, list = 25%, signal = 80% WELCSH_BRCA1_TARGETS_1_DN 103 −0.50022 −2.24119 0 2.53E−04 0.01 5398 tags = 49%, list = 25%, signal = 64% ZHAN_MULTIPLE_MYELOMA_PR_UP 30 −0.66657 −2.23876 0 2.49E−04 0.01 5457 tags = 73%, list = 25%, signal = 98% SCHLOSSER_MYC_TARGETS_AND_SERUM_RESPONSE_(—) 42 −0.5993 −2.23838 0 2.45E−04 0.01 7170 tags = 79%, list = 33%, UP signal = 117% KANG_DOXORUBICIN_RESISTANCE_UP 42 −0.60911 −2.23058 0 2.41E−04 0.01 6063 tags = 79%, list = 28%, signal = 108% REACTOME_TRANSCRIPTION_OF_THE_HIV_GENOME 56 −0.55479 −2.22406 0 2.37E−04 0.01 8431 tags = 77%, list = 39%, signal = 125% YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_(—) 162 −0.46632 −2.22323 0 2.34E−04 0.01 8156 tags = 58%, list = 37%, CLUSTER_17 signal = 92% KEGG_AMINOACYL_TRNA_BIOSYNTHESIS 29 −0.65833 −2.22232 0 2.30E−04 0.01 5501 tags = 76%, list = 25%, signal = 101% BIOCARTA_CYTOKINE_PATHWAY 19 −0.73463 −2.22217 0 2.27E−04 0.01 1999 tags = 58%, list = 9%, signal = 64% VECCHI_GASTRIC_CANCER_EARLY_UP 312 −0.43099 −2.22032 0 2.24E−04 0.01 5572 tags = 49%, list = 25%, signal = 65% FINETTI_BREAST_CANCER_KINOME_RED 15 −0.77765 −2.22007 0 2.21E−04 0.01 3773 tags = 80%, list = 17%, signal = 97% SONG_TARGETS_OF_IE86_CMV_PROTEIN 42 −0.59892 −2.2135 0 2.61E−04 0.011 6296 tags = 69%, list = 29%, signal = 97% FINETTI_BREAST_CANCER_BASAL_VS_LUMINAL 15 −0.77765 −2.21228 0 2.58E−04 0.011 3773 tags = 80%, list = 17%, signal = 97% FERREIRA_EWINGS_SARCOMA_UNSTABLE_VS_STABLE_(—) 110 −0.48933 −2.21168 0 2.54E−04 0.011 6401 tags = 62%, list = 29%, UP signal = 87% REACTOME_ACTIVATION_OF_ATR_IN_RESPONSE_TO_(—) 35 −0.63192 −2.21151 0 2.51E−04 0.011 6833 tags = 80%, list = 31%, REPLICATION_STRESS signal = 116% REACTOME_TRNA_AMINOACYLATION 28 −0.65329 −2.20926 0 2.47E−04 0.011 5918 tags = 79%, list = 27%, signal = 108% REACTOME_REV_MEDIATED_NUCLEAR_EXPORT_OF_(—) 31 −0.63725 −2.2092 0 2.44E−04 0.011 6272 tags = 74%, list = 29%, HIV1_RNA signal = 104% PUJANA_BRCA2_PCC_NETWORK 354 −0.42091 −2.19518 0 3.01E−04 0.014 6984 tags = 55%, list = 32%, signal = 80% PUJANA_BREAST_CANCER_WITH_BRCA1_MUTATED_(—) 48 −0.57048 −2.19223 0 2.97E−04 0.014 7650 tags = 69%, list = 35%, UP signal = 105% BENPORATH_CYCLING_GENES 487 −0.40496 −2.18482 0 2.94E−04 0.014 6063 tags = 47%, list = 28%, signal = 63% TARTE_PLASMA_CELL_VS_PLASMABLAST_DN 264 −0.43192 −2.18475 0 2.90E−04 0.014 6794 tags = 50%, list = 31%, signal = 72% ZHANG_BREAST_CANCER_PROGENITORS_UP 356 −0.41639 −2.18359 0 2.86E−04 0.014 5110 tags = 39%, list = 23%, signal = 50% MOLENAAR_TARGETS_OF_CCND1_AND_CDK4_DN 38 −0.59147 −2.18357 0 2.83E−04 0.014 5413 tags = 68%, list = 25%, signal = 91% CHEMNITZ_RESPONSE_TO_PROSTAGLANDIN_E2_UP 105 −0.49243 −2.18272 0 2.80E−04 0.014 5603 tags = 53%, list = 26%, signal = 71% CHIANG_LIVER_CANCER_SUBCLASS_PROLIFERATION_(—) 126 −0.48551 −2.17998 0 2.94E−04 0.015 6037 tags = 59%, list = 28%, UP signal = 81% MORI_IMMATURE_B_LYMPHOCYTE_DN 51 −0.56172 −2.17923 0 3.09E−04 0.016 4901 tags = 55%, list = 22%, signal = 71% LI_WILMS_TUMOR_VS_FETAL_KIDNEY_1_DN 143 −0.47552 −2.17785 0 3.58E−04 0.019 6032 tags = 57%, list = 28%, signal = 79% REACTOME_G1_S_TRANSITION 95 −0.49882 −2.16889 0 4.24E−04 0.023 8423 tags = 76%, list = 38%, signal = 123% REACTOME_ORC1_REMOVAL_FROM_CHROMATIN 62 −0.53445 −2.16413 0 4.19E−04 0.023 8423 tags = 76%, list = 38%, signal = 123% REACTOME_VPR_MEDIATED_NUCLEAR_IMPORT_OF_PICS 31 −0.62822 −2.16243 0 4.31E−04 0.024 6272 tags = 71%, list = 29%, signal = 99% MARZEC_IL2_SIGNALING_UP 95 −0.5007 −2.1622 0 4.27E−04 0.024 3897 tags = 46%, list = 18%, signal = 56% LEE_EARLY_T_LYMPHOCYTE_UP 62 −0.53445 −2.16142 0 4.22E−04 0.024 6063 tags = 66%, list = 28%, signal = 91% BOYAULT_LIVER_CANCER_SUBCLASS_G3_UP 141 −0.46084 −2.1547 0 4.17E−04 0.024 7315 tags = 61%, list = 33%, signal = 91% REACTOME_TRANSPORT_OF_THE_SLBP_INDEPENDENT_(—) 31 −0.62469 −2.1546 0 4.13E−04 0.024 6272 tags = 71%, list = 29%, MATURE_MRNA signal = 99% REACTOME_M_G1_TRANSITION 60 −0.53293 −2.15376 0 4.09E−04 0.024 8423 tags = 75%, list = 38%, signal = 122% REACTOME_FORMATION_AND_MATURATION_OF_(—) 124 −0.46416 −2.14877 0 4.04E−04 0.024 7557 tags = 61%, list = 35%, MRNA_TRANSCRIPT signal = 93% CROONQUIST_NRAS_VS_STROMAL_STIMULATION_DN 67 −0.52518 −2.14495 0 4.00E−04 0.024 4737 tags = 52%, list = 22%, signal = 66% REACTOME_ACTIVATION_OF_THE_PRE_REPLICATIVE_(—) 27 −0.64535 −2.13937 0 4.43E−04 0.027 6833 tags = 85%, list = 31%, COMPLEX signal = 124% FURUKAWA_DUSP6_TARGETS_PCI35_DN 53 −0.54107 −2.13646 0 4.70E−04 0.029 5506 tags = 64%, list = 25%, signal = 86% REACTOME_NEP_NS2_INTERACTS_WITH_THE_(—) 29 −0.63219 −2.13521 0 4.65E−04 0.029 6272 tags = 72%, list = 29%, CELLULAR_EXPORT_MACHINERY signal = 101% SARRIO_EPITHELIAL_MESENCHYMAL_TRANSITION_UP 15 −0.73215 −2.13413 0 4.61E−04 0.029 5555 tags = 93%, list = 25%, signal = 125% KEGG_HOMOLOGOUS_RECOMBINATION 26 −0.65195 −2.13209 0 4.71E−04 0.03 4302 tags = 54%, list = 20%, signal = 67% REACTOME_TRANSPORT_OF_RIBONUCLEOPROTEINS_(—) 29 −0.62504 −2.12057 0 5.88E−04 0.038 7635 tags = 83%, list = 35%, INTO_THE_HOST_NUCLEUS signal = 127% REACTOME_TRANSCRIPTION_COUPLED_NER 44 −0.55892 −2.11943 0 5.82E−04 0.038 8892 tags = 86%, list = 41%, signal = 145% REACTOME_NUCLEAR_IMPORT_OF_REV_PROTEIN 30 −0.63441 −2.11724 0 5.77E−04 0.038 7635 tags = 87%, list = 35%, signal = 133% KAUFFMANN_DNA_REPLICATION_GENES 122 −0.46254 −2.11386 0 6.28E−04 0.042 6879 tags = 54%, list = 31%, signal = 78% MITSIADES_RESPONSE_TO_APLIDIN_DN 203 −0.4327 −2.11313 0 6.22E−04 0.042 6448 tags = 51%, list = 29%, signal = 71% MOOTHA_HUMAN_MITODB_6_2002 390 −0.40354 −2.11231 0 6.17E−04 0.042 6758 tags = 46%, list = 31%, signal = 66% REACTOME_PROCESSING_OF_CAPPED_INTRON_(—) 112 −0.48203 −2.11184 0 6.11E−04 0.042 7635 tags = 64%, list = 35%, CONTAINING_PRE_MRNA signal = 98% PENG_GLUTAMINE_DEPRIVATION_DN 70 −0.51196 −2.11181 0 6.05E−04 0.042 6354 tags = 59%, list = 29%, signal = 82% REACTOME_HIV1_TRANSCRIPTION_INITIATION 39 −0.57113 −2.1081 0 6.28E−04 0.044 8247 tags = 79%, list = 38%, signal = 127% RHODES_UNDIFFERENTIATED_CANCER 57 −0.52455 −2.10806 0 6.22E−04 0.044 7746 tags = 67%, list = 35%, signal = 103% TANG_SENESCENCE_TP53_TARGETS_DN 35 −0.57539 −2.10783 0 6.17E−04 0.044 5348 tags = 63%, list = 24%, signal = 83% BIOCARTA_ATRBRCA_PATHWAY 20 −0.67215 −2.10398 0 6.38E−04 0.046 5247 tags = 70%, list = 24%, signal = 92% MORI_LARGE_PRE_BII_LYMPHOCYTE_UP 53 −0.54205 −2.10142 0 6.47E−04 0.047 7289 tags = 72%, list = 33%, signal = 107% TIEN_INTESTINE_PROBIOTICS_24HR_UP 455 −0.39298 −2.0885 0 8.14E−04 0.058 7207 tags = 53%, list = 33%, signal = 77% KEGG_BASAL_TRANSCRIPTION_FACTORS 31 −0.59988 −2.08011 0 8.59E−04 0.062 5796 tags = 68%, list = 26%, signal = 92% PODAR_RESPONSE_TO_ADAPHOSTIN_DN 16 −0.7055 −2.07696 0 9.04E−04 0.065 3479 tags = 63%, list = 16%, signal = 74% REACTOME_REGULATION_OF_GLUCOKINASE_BY_(—) 29 −0.60978 −2.0751 0 9.22E−04 0.067 6272 tags = 72%, list = 29%, GLUCOKINASE_REGULATORY_PROTEIN signal = 101% AMUNDSON_GAMMA_RADIATION_RESPONSE 32 −0.59312 −2.07276 0 9.40E−04 0.069 6032 tags = 66%, list = 28%, signal = 90% MISSIAGLIA_REGULATED_BY_METHYLATION_DN 89 −0.48206 −2.07014 0 9.84E−04 0.073 6873 tags = 58%, list = 31%, signal = 85% SHAFFER_IRF4_TARGETS_IN_ACTIVATED_B_LYMPHOCYTE 74 −0.49013 −2.06892 0 9.75E−04 0.073 4857 tags = 49%, list = 22%, signal = 62% REACTOME_EXTENSION_OF_TELOMERES 23 −0.65295 −2.066 0 0.001017 0.076 5837 tags = 74%, list = 27%, signal = 101% DIRMEIER_LMP1_RESPONSE_LATE_UP 42 −0.5521 −2.05234 0 0.001257 0.092 5294 tags = 45%, list = 24%, signal = 60% KEGG_DNA_REPLICATION 32 −0.60017 −2.05097 0 0.001259 0.093 6929 tags = 72%, list = 32%, signal = 105% GARY_CD5_TARGETS_DN 341 −0.39679 −2.04839 0 0.001286 0.096 7114 tags = 55%, list = 32%, signal = 81% MARSON_FOXP3_TARGETS_DN 39 −0.551 −2.04432 0 0.001348 0.101 4412 tags = 46%, list = 20%, signal = 58% MORI_EMU_MYC_LYMPHOMA_BY_ONSET_TIME_UP 96 −0.47001 −2.04192 0 0.001362 0.103 6328 tags = 55%, list = 29%, signal = 77% GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_(—) 37 −0.56283 −2.03863 0 0.001422 0.109 4401 tags = 59%, list = 20%, TURQUOISE_DN signal = 74% KEGG_ASTHMA 15 −0.71208 −2.03735 0 0.001518 0.118 1999 tags = 47%, list = 9%, signal = 51% EGUCHI_CELL_CYCLE_RB1_TARGETS 18 −0.68811 −2.03727 0 0.001506 0.118 4559 tags = 72%, list = 21%, signal = 91% SCHLOSSER_MYC_TARGETS_AND_SERUM_RESPONSE_(—) 40 −0.55101 −2.03688 0 0.001507 0.119 5731 tags = 60%, list = 26%, DN signal = 81% ELVIDGE_HYPOXIA_DN 117 −0.45344 −2.0311 0 0.001622 0.128 5371 tags = 47%, list = 25%, signal = 62% REACTOME_DNA_STRAND_ELONGATION 26 −0.62331 −2.031 0.002198 0.001622 0.129 6770 tags = 77%, list = 31%, signal = 111% REACTOME_TRANSCRIPTION 140 −0.43535 −2.03019 0 0.001621 0.129 7557 tags = 60%, list = 35%, signal = 91% MOOTHA_MITOCHONDRIA 402 −0.38548 −2.02633 0 0.001758 0.141 6758 tags = 46%, list = 31%, signal = 65% DANG_MYC_TARGETS_UP 109 −0.45162 −2.02125 0 0.001857 0.15 7245 tags = 55%, list = 33%, signal = 82% DANG_REGULATED_BY_MYC_UP 59 −0.5127 −2.02065 0 0.001843 0.15 6439 tags = 59%, list = 29%, signal = 84% REACTOME_HOST_INTERACTIONS_OF_HIV_FACTORS 115 −0.44796 −2.01819 0 0.001851 0.152 8903 tags = 68%, list = 41%, signal = 114% ZHANG_RESPONSE_TO_CANTHARIDIN_DN 49 −0.52917 −2.01757 0 0.001838 0.152 6558 tags = 59%, list = 30%, signal = 84% TONG_INTERACT_WITH_PTTG1 39 −0.54688 −2.01355 0 0.001933 0.159 5056 tags = 49%, list = 23%, signal = 63% BIOCARTA_INFLAM_PATHWAY 25 −0.61727 −2.0126 0 0.001942 0.16 1999 tags = 40%, list = 9%, signal = 44% REACTOME_CDT1_ASSOCIATION_WITH_THE_CDC6_(—) 51 −0.51868 −2.0036 0 0.00208 0.173 8423 tags = 73%, list = 38%, ORC_ORIGIN_COMPLEX signal = 118% KEGG_PYRIMIDINE_METABOLISM 86 −0.46227 −1.99674 0 0.002332 0.19 4372 tags = 44%, list = 20%, signal = 55% RHEIN_ALL_GLUCOCORTICOID_THERAPY_DN 315 −0.38684 −1.99663 0 0.002316 0.19 7650 tags = 54%, list = 35%, signal = 82% BENPORATH_ES_1 299 −0.38787 −1.9956 0 0.002343 0.193 5302 tags = 41%, list = 24%, signal = 54% LY_AGING_OLD_DN 43 −0.53325 −1.99505 0 0.002348 0.194 5064 tags = 56%, list = 23%, signal = 72% REACTOME_REGULATION_OF_APC_ACTIVATORS_(—) 67 −0.48117 −1.99433 0 0.002342 0.195 8903 tags = 72%, list = 41%, BETWEEN_G1_S_AND_EARLY_ANAPHASE signal = 120% MARTORIATI_MDM4_TARGETS_NEUROEPITHELIUM_UP 89 −0.46873 −1.99372 0 0.002347 0.197 4616 tags = 35%, list = 21%, signal = 44% CHIANG_LIVER_CANCER_SUBCLASS_UNANNOTATED_(—) 142 −0.42418 −1.99351 0 0.002352 0.199 6920 tags = 49%, list = 32%, DN signal = 72% REACTOME_CYCLIN_E_ASSOCIATED_EVENTS_DURING_(—) 56 −0.50105 −1.99109 0 0.002428 0.208 8423 tags = 70%, list = 38%, G1_S_TRANSITION signal = 113% CHANG_CYCLING_GENES 37 −0.55801 −1.98899 0 0.002473 0.214 4106 tags = 59%, list = 19%, signal = 73% RICKMAN_METASTASIS_UP 224 −0.39927 −1.97561 0 0.003032 0.258 5792 tags = 42%, list = 26%, signal = 56% DAIRKEE_TERT_TARGETS_UP 254 −0.3908 −1.9717 0 0.003174 0.271 5075 tags = 33%, list = 23%, signal = 42% ZHAN_MULTIPLE_MYELOMA_SUBGROUPS 26 −0.60061 −1.96794 0.002353 0.003313 0.283 6794 tags = 62%, list = 31%, signal = 89% UDAYAKUMAR_MED1_TARGETS_UP 108 −0.44358 −1.96757 0 0.003312 0.285 4110 tags = 38%, list = 19%, signal = 47% BORCZUK_MALIGNANT_MESOTHELIOMA_UP 258 −0.39069 −1.96646 0 0.003388 0.294 7491 tags = 48%, list = 34%, signal = 72% STEIN_ESRRA_TARGETS_RESPONSIVE_TO_ESTROGEN_(—) 36 −0.54912 −1.9664 0.002242 0.003377 0.295 4568 tags = 50%, list = 21%, DN signal = 63% NADERI_BREAST_CANCER_PROGNOSIS_UP 33 −0.56192 −1.96618 0 0.003365 0.296 3686 tags = 52%, list = 17%, signal = 62% MOREAUX_MULTIPLE_MYELOMA_BY_TACI_DN 102 −0.44369 −1.96265 0 0.003508 0.306 7245 tags = 54%, list = 33%, signal = 80% REACTOME_CYTOSOLIC_TRNA_AMINOACYLATION 18 −0.65663 −1.95881 0.002132 0.003581 0.314 5918 tags = 83%, list = 27%, signal = 114% BOYLAN_MULTIPLE_MYELOMA_C_D_UP 110 −0.43955 −1.95861 0 0.003559 0.314 6352 tags = 49%, list = 29%, signal = 69% GRADE_COLON_AND_RECTAL_CANCER_UP 203 −0.39763 −1.95855 0 0.003537 0.314 6949 tags = 50%, list = 32%, signal = 73% FAELT_B_CLL_WITH_VH3_21_UP 37 −0.5493 −1.95553 0 0.003591 0.32 6063 tags = 57%, list = 28%, signal = 78% KEGG_SPLICEOSOME 92 −0.44834 −1.95543 0 0.003588 0.321 7655 tags = 62%, list = 35%, signal = 95% KIM_WT1_TARGETS_DN 359 −0.37271 −1.95293 0 0.003679 0.33 4941 tags = 35%, list = 23%, signal = 44% PENG_RAPAMYCIN_RESPONSE_DN 55 −0.49874 −1.94479 0 0.003932 0.35 7835 tags = 65%, list = 36%, signal = 102% GOLDRATH_ANTIGEN_RESPONSE 329 −0.3714 −1.94272 0 0.004009 0.36 4135 tags = 33%, list = 19%, signal = 41% FOURNIER_ACINAR_DEVELOPMENT_LATE_DN 18 −0.64974 −1.9417 0.002242 0.004049 0.364 4508 tags = 56%, list = 21%, signal = 70% REACTOME_GENE_EXPRESSION 333 −0.37499 −1.9391 0 0.004245 0.378 7581 tags = 49%, list = 35%, signal = 74% SMITH_TERT_TARGETS_UP 117 −0.42979 −1.9385 0 0.004229 0.378 5561 tags = 41%, list = 25%, signal = 55% REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION_(—) 27 −0.57971 −1.93649 0 0.00432 0.385 7276 tags = 85%, list = 33%, INITIATION signal = 127% WEST_ADRENOCORTICAL_TUMOR_UP 251 −0.38353 −1.9344 0 0.004402 0.392 6315 tags = 46%, list = 29%, signal = 64% MONNIER_POSTRADIATION_TUMOR_ESCAPE_UP 347 −0.37413 −1.93378 0 0.004395 0.393 5548 tags = 43%, list = 25%, signal = 56% REACTOME_ELONGATION_AND_PROCESSING_OF_(—) 106 −0.4328 −1.93342 0 0.004388 0.395 9169 tags = 74%, list = 42%, CAPPED_TRANSCRIPTS signal = 126% REACTOME_SCF_SKP2_MEDIATED_DEGRADATION_(—) 50 −0.50927 −1.93218 0 0.004389 0.398 8903 tags = 76%, list = 41%, OF_P27_P21 signal = 128% REACTOME_HIV1_TRANSCRIPTION_ELONGATION 38 −0.53048 −1.93192 0 0.004399 0.401 8812 tags = 79%, list = 40%, signal = 132% POMEROY_MEDULLOBLASTOMA_PROGNOSIS_DN 37 −0.53422 −1.93093 0.002433 0.004427 0.403 4941 tags = 38%, list = 23%, signal = 49% MOREAUX_B_LYMPHOCYTE_MATURATION_BY_TACI_(—) 33 −0.54589 −1.93023 0 0.004427 0.404 7463 tags = 73%, list = 34%, DN signal = 110% KEGG_ALLOGRAFT_REJECTION 16 −0.66098 −1.92958 0 0.004412 0.405 1560 tags = 44%, list = 7%, signal = 47% REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION_(—) 19 −0.6396 −1.92587 0 0.004549 0.412 6903 tags = 84%, list = 32%, INITIATION_FROM_TYPE_2_PROMOTER signal = 123% REACTOME_INFLUENZA_LIFE_CYCLE 120 −0.42562 −1.92572 0 0.004533 0.413 7779 tags = 37%, list = 36%, signal = 57% REACTOME_GLUCOSE_TRANSPORT 38 −0.53865 −1.92421 0 0.004568 0.416 6272 tags = 66%, list = 29%, signal = 92% LASTOWSKA_NEUROBLASTOMA_COPY_NUMBER_UP 138 −0.41264 −1.92201 0 0.004635 0.425 6262 tags = 48%, list = 29%, signal = 67% SCIAN_CELL_CYCLE_TARGETS_OF_TP53_AND_TP73_DN 22 −0.61497 −1.92181 0 0.004627 0.426 6653 tags = 77%, list = 30%, signal = 111% JAIN_NFKB_SIGNALING 64 −0.48498 −1.92171 0 0.004602 0.426 5141 tags = 44%, list = 23%, signal = 57% HORIUCHI_WTAP_TARGETS_DN 244 −0.38519 −1.92097 0 0.00461 0.428 6174 tags = 50%, list = 28%, signal = 68% LY_AGING_MIDDLE_DN 15 −0.67338 −1.91334 0 0.005071 0.456 4941 tags = 73%, list = 23%, signal = 95% BERENJENO_TRANSFORMED_BY_RHOA_FOREVER_DN 29 −0.55886 −1.90259 0 0.005696 0.496 3614 tags = 38%, list = 17%, signal = 45% BLUM_RESPONSE_TO_SALIRASIB_UP 211 −0.38676 −1.90016 0 0.005837 0.508 3107 tags = 26%, list = 14%, signal = 30% MARTORIATI_MDM4_TARGETS_FETAL_LIVER_UP 91 −0.43519 −1.89764 0 0.005936 0.515 3944 tags = 31%, list = 18%, signal = 37% REACTOME_DOUBLE_STRAND_BREAK_REPAIR 20 −0.62559 −1.89719 0.004255 0.005929 0.516 5837 tags = 70%, list = 27%, signal = 95% KIM_GASTRIC_CANCER_CHEMOSENSITIVITY 78 −0.44364 −1.89423 0 0.006027 0.522 3650 tags = 38%, list = 17%, signal = 46% SCHLOSSER_MYC_AND_SERUM_RESPONSE_SYNERGY 29 −0.54597 −1.88921 0 0.006411 0.546 4807 tags = 48%, list = 22%, signal = 62% REACTOME_DUAL_INCISION_REACTION_IN_TC_NER 28 −0.55454 −1.88646 0 0.006559 0.556 8812 tags = 86%, list = 40%, signal = 143% RICKMAN_TUMOR_DIFFERENTIATED_MODERATELY_(—) 31 −0.53885 −1.87914 0 0.006947 0.577 5365 tags = 58%, list = 25%, VS_POORLY_DN signal = 77% WONG_MITOCHONDRIA_GENE_MODULE 199 −0.38573 −1.87702 0 0.007099 0.587 7076 tags = 44%, list = 32%, signal = 64% MARTINEZ_RESPONSE_TO_TRABECTEDIN_DN 194 −0.38764 −1.87447 0 0.00732 0.603 7218 tags = 45%, list = 33%, signal = 66% DAZARD_UV_RESPONSE_CLUSTER_G2 17 −0.6373 −1.87043 0 0.007678 0.624 3340 tags = 53%, list = 15%, signal = 62% BIOCARTA_ATM_PATHWAY 19 −0.61513 −1.86847 0 0.007825 0.636 4235 tags = 53%, list = 19%, signal = 65% RAMALHO_STEMNESS_UP 185 −0.3878 −1.86734 0 0.00787 0.641 6413 tags = 49%, list = 29%, signal = 68% REACTOME_CDC20_PHOSPHO_APC_MEDIATED_(—) 60 −0.46466 −1.8658 0 0.007931 0.644 8446 tags = 65%, list = 39%, DEGRADATION_OF_CYCLIN_A signal = 106% RICKMAN_TUMOR_DIFFERENTIATED_MODERATELY_(—) 31 −0.53885 −1.86463 0 0.008065 0.655 5365 tags = 58%, list = 25%, VS_POORLY_UP signal = 77% REACTOME_FORMATION_OF_THE_EARLY_ELONGATION_(—) 29 −0.54611 −1.86136 0.002342 0.008358 0.668 8812 tags = 83%, list = 40%, COMPLEX signal = 138% FARMER_BREAST_CANCER_CLUSTER_2 29 −0.54068 −1.85871 0.006757 0.00861 0.677 6868 tags = 76%, list = 31%, signal = 110% KEGG_CELL_CYCLE 117 −0.4118 −1.85676 0 0.008755 0.685 6324 tags = 46%, list = 29%, signal = 65% REACTOME_LAGGING_STRAND_SYNTHESIS 18 −0.61461 −1.85531 0.002288 0.008883 0.696 5837 tags = 67%, list = 27%, signal = 91% BIOCARTA_G2_PATHWAY 23 −0.58922 −1.85412 0.002198 0.008988 0.704 2092 tags = 39%, list = 10%, signal = 43% VERNELL_RETINOBLASTOMA_PATHWAY_UP 35 −0.51946 −1.85328 0 0.009063 0.709 4507 tags = 46%, list = 21%, signal = 57% KEGG_RNA_POLYMERASE 25 −0.57055 −1.85044 0.006711 0.009299 0.719 8812 tags = 88%, list = 40%, signal = 147% REACTOME_SCF_BETA_TRCP_MEDIATED_DEGRADATION_(—) 46 −0.48745 −1.85016 0.002347 0.009277 0.72 8903 tags = 74%, list = 41%, OF_EMI1 signal = 124% REACTOME_RNA_POL_II_CTD_PHOSPHORYLATION_AND_(—) 26 −0.55486 −1.84559 0.002247 0.009719 0.736 8812 tags = 85%, list = 40%, INTERACTION_WITH_CE signal = 141% REACTOME_NUCLEOTIDE_EXCISION_REPAIR 49 −0.47111 −1.84298 0 0.009977 0.751 5861 tags = 53%, list = 27%, signal = 72% KOKKINAKIS_METHIONINE_DEPRIVATION_48HR_DN 58 −0.46731 −1.84273 0 0.009966 0.753 1826 tags = 21%, list = 8%, signal = 23% REACTOME_PHOSPHOLIPASE_CMEDIATED_CASCADE 22 −0.56055 −1.83603 0 0.010787 0.791 2299 tags = 32%, list = 11%, signal = 36% LINDGREN_BLADDER_CANCER_CLUSTER_1_DN 307 −0.35516 −1.83076 0 0.011328 0.801 6296 tags = 45%, list = 29%, signal = 62% CHANG_CORE_SERUM_RESPONSE_UP 56 −0.46454 −1.82947 0.002315 0.011397 0.807 4678 tags = 39%, list = 21%, signal = 50% REACTOME_CHOLESTEROL_BIOSYNTHESIS 20 −0.5839 −1.82928 0.002183 0.011366 0.808 5072 tags = 55%, list = 23%, signal = 72% ROYLANCE_BREAST_CANCER_16Q_COPY_NUMBER_UP 29 −0.53691 −1.82878 0.004577 0.01137 0.81 4716 tags = 48%, list = 22%, signal = 61% BENPORATH_ES_2 27 −0.55087 −1.81839 0.004484 0.01288 0.856 5302 tags = 59%, list = 24%, signal = 78% AMIT_EGF_RESPONSE_120_HELA 55 −0.46762 −1.81837 0 0.012822 0.856 4950 tags = 42%, list = 23%, signal = 54% COLDREN_GEFITINIB_RESISTANCE_UP 59 −0.45676 −1.81786 0 0.012833 0.859 5037 tags = 49%, list = 23%, signal = 64% TIAN_TNF_SIGNALING_VIA_NFKB 20 −0.59467 −1.81746 0.008584 0.012824 0.86 2350 tags = 30%, list = 11%, signal = 34% REACTOME_P53_INDEPENDENT_DNA_DAMAGE_(—) 42 −0.47587 −1.80875 0.006993 0.013778 0.877 8903 tags = 71%, list = 41%, RESPONSE signal = 120% MOREIRA_RESPONSE_TO_TSA_UP 26 −0.54433 −1.80792 0 0.013807 0.879 8222 tags = 73%, list = 38%, signal = 117% PUJANA_BREAST_CANCER_LIT_INT_NETWORK 93 −0.42623 −1.80673 0 0.013938 0.883 5554 tags = 45%, list = 25%, signal = 60% BONOME_OVARIAN_CANCER_POOR_SURVIVAL_DN 15 −0.63225 −1.80075 0.004494 0.014705 0.895 4297 tags = 47%, list = 20%, signal = 58% REACTOME_FGFR_LIGAND_BINDING_AND_ACTIVATION 26 −0.54964 −1.80033 0.002141 0.014709 0.896 2299 tags = 31%, list = 11%, signal = 34% REACTOME_SIGNALING_BY_WNT 56 −0.45072 −1.79818 0 0.015068 0.902 8903 tags = 63%, list = 41%, signal = 105% SENGUPTA_NASOPHARYNGEAL_CARCINOMA_UP 212 −0.37124 −1.79813 0 0.015003 0.902 5102 tags = 42%, list = 23%, signal = 54% REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION_(—) 20 −0.58695 −1.79724 0.002247 0.015046 0.904 5861 tags = 75%, list = 27%, INITIATION_FROM_TYPE_3_PROMOTER signal = 102% HOFMANN_CELL_LYMPHOMA_UP 35 −0.51003 −1.79645 0 0.015047 0.904 5796 tags = 51%, list = 26%, signal = 70% REACTOME_TAT_MEDIATED_HIV1_ELONGATION_(—) 28 −0.53564 −1.79353 0.002179 0.015392 0.912 8812 tags = 79%, list = 40%, ARREST_AND_RECOVERY signal = 131% REACTOME_E2F_MEDIATED_REGULATION_OF_DNA_(—) 29 −0.53228 −1.7906 0 0.015682 0.918 3495 tags = 52%, list = 16%, REPLICATION signal = 61% IVANOVA_HEMATOPOIESIS_EARLY_PROGENITOR 104 −0.40837 −1.7891 0 0.015873 0.919 5399 tags = 43%, list = 25%, signal = 57% ELVIDGE_HIF1A_AND_HIF2A_TARGETS_UP 33 −0.51171 −1.78889 0 0.015819 0.919 4163 tags = 45%, list = 19%, signal = 56% KEGG_NUCLEOTIDE_EXCISION_REPAIR 43 −0.47622 −1.78586 0.002342 0.01618 0.922 5837 tags = 51%, list = 27%, signal = 70% RICKMAN_TUMOR_DIFFERENTIATED_WELL_VS_(—) 84 −0.41982 −1.78206 0 0.016747 0.929 2380 tags = 26%, list = 11%, MODERATELY_DN signal = 29% REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION_(—) 21 −0.56692 −1.78095 0.006787 0.016864 0.929 3988 tags = 43%, list = 18%, INITIATION signal = 52% NAKAYAMA_SOFT_TISSUE_TUMORS_PCA2_UP 75 −0.43046 −1.78083 0 0.016807 0.929 5413 tags = 51%, list = 25%, signal = 67% YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_(—) 70 −0.42897 −1.77415 0 0.018068 0.942 6043 tags = 53%, list = 28%, CLUSTER_16 signal = 73% HOFFMANN_IMMATURE_TO_MATURE_B_LYMPHOCYTE_(—) 27 −0.53522 −1.77305 0.002174 0.018146 0.943 2076 tags = 33%, list = 9%, DN signal = 37% KEGG_PROTEASOME 42 −0.47505 −1.77153 0 0.018324 0.947 8666 tags = 69%, list = 40%, signal = 114% REACTOME_MRNA_3_END_PROCESSING 30 −0.52256 −1.77128 0.006356 0.018337 0.947 9277 tags = 83%, list = 42%, signal = 144% REACTOME_MICRORNA_BIOGENESIS 18 −0.58374 −1.77095 0.004184 0.018324 0.947 8812 tags = 94%, list = 40%, signal = 158% ELVIDGE_HIF1A_TARGETS_UP 51 −0.46192 −1.77012 0 0.018407 0.95 4807 tags = 47%, list = 22%, signal = 60% REACTOME_TELOMERE_MAINTENANCE 35 −0.49494 −1.76955 0.002309 0.018463 0.95 5837 tags = 63%, list = 27%, signal = 86% GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_(—) 88 −0.40513 −1.76935 0 0.018438 0.951 5516 tags = 41%, list = 25%, BLUE_UP signal = 54% BRUECKNER_TARGETS_OF_MIRLET7A3_DN 58 −0.44814 −1.76909 0 0.018383 0.951 4542 tags = 33%, list = 21%, signal = 41% HENDRICKS_SMARCA4_TARGETS_UP 37 −0.49018 −1.76748 0 0.018566 0.953 3413 tags = 32%, list = 16%, signal = 38% KEGG_BASE_EXCISION_REPAIR 31 −0.51872 −1.76719 0.007407 0.01856 0.953 5913 tags = 58%, list = 27%, signal = 79% ELVIDGE_HYPOXIA_BY_DMOG_DN 48 −0.45245 −1.76658 0.002387 0.018647 0.955 4662 tags = 46%, list = 21%, signal = 58% KRIGE_AMINO_ACID_DEPRIVATION 24 −0.53613 −1.75146 0.002203 0.021451 0.971 2795 tags = 38%, list = 13%, signal = 43% GRAHAM_CML_QUIESCENT_VS_CML_DIVIDING_UP 18 −0.59264 −1.75123 0.004376 0.021433 0.971 3128 tags = 44%, list = 14%, signal = 52% REACTOME_MRNA_SPLICING 81 −0.42193 −1.75088 0 0.021433 0.971 9158 tags = 75%, list = 42%, signal = 129% SCIBETTA_KDM5B_TARGETS_DN 62 −0.4322 −1.74733 0.00232 0.021984 0.974 6859 tags = 60%, list = 31%, signal = 87% WEST_ADRENOCORTICAL_TUMOR_MARKERS_UP 19 −0.57446 −1.74619 0.004525 0.022091 0.975 6004 tags = 79%, list = 27%, signal = 109% NAGASHIMA_EGF_SIGNALING_UP 51 −0.4524 −1.74565 0.002326 0.022148 0.975 4328 tags = 41%, list = 20%, signal = 51% LY_AGING_PREMATURE_DN 22 −0.54918 −1.74559 0.006303 0.02208 0.975 5064 tags = 55%, list = 23%, signal = 71% REACTOME_VIF_MEDIATED_DEGRADATION_OF_(—) 45 −0.45878 −1.74448 0.002273 0.02225 0.975 8903 tags = 69%, list = 41%, APOBEC3G signal = 116% WANG_SMARCE1_TARGETS_DN 268 −0.34773 −1.74421 0 0.022213 0.975 4223 tags = 29%, list = 19%, signal = 35% REACTOME_RNA_POLYMERASE_I_III_AND_(—) 69 −0.42423 −1.74093 0 0.022727 0.978 6005 tags = 52%, list = 27%, MITOCHONDRIAL_TRANSCRIPTION signal = 72% BUYTAERT_PHOTODYNAMIC_THERAPY_STRESS_DN 485 −0.32386 −1.74085 0 0.022653 0.978 5555 tags = 36%, list = 25%, signal = 47% BROWNE_HCMV_INFECTION_24HR_UP 133 −0.37862 −1.74079 0 0.022578 0.978 6153 tags = 46%, list = 28%, signal = 63% REACTOME_SHCMEDIATED_CASCADE 21 −0.55619 −1.74072 0.00883 0.022505 0.978 2299 tags = 29%, list = 11%, signal = 32% BIOCARTA_SPRY_PATHWAY 18 −0.57942 −1.74034 0.006623 0.022501 0.978 1759 tags = 28%, list = 8%, signal = 30% REACTOME_ABORTIVE_ELONGATION_OF_HIV1_(—) 20 −0.5675 −1.74029 0.013575 0.022422 0.978 9169 tags = 90%, list = 42%, TRANSCRIPT_IN_THE_ABSENCE_OF_TAT signal = 155% KEGG_MISMATCH_REPAIR 22 −0.55825 −1.73989 0.006522 0.022408 0.978 8892 tags = 86%, list = 41%, signal = 145% REACTOME_BASE_EXCISION_REPAIR 16 −0.59901 −1.73733 0.011287 0.022865 0.979 6552 tags = 69%, list = 30%, signal = 98% DOANE_BREAST_CANCER_CLASSES_DN 29 −0.50954 −1.73694 0.006579 0.022861 0.98 2768 tags = 28%, list = 13%, signal = 32% LIU_SOX4_TARGETS_DN 241 −0.3473 −1.7365 0 0.022884 0.982 6368 tags = 39%, list = 29%, signal = 54% BOYLAN_MULTIPLE_MYELOMA_D_UP 83 −0.4079 −1.73612 0 0.022886 0.982 5005 tags = 40%, list = 23%, signal = 51% ZHANG_RESPONSE_TO_IKK_INHIBITOR_AND_TNF_DN 69 −0.41797 −1.73513 0.005249 0.023017 0.983 2419 tags = 29%, list = 11%, signal = 32% SHIPP_DLBCL_VS_FOLLICULAR_LYMPHOMA_UP 41 −0.47072 −1.73454 0.008511 0.023047 0.983 7538 tags = 76%, list = 34%, signal = 115% AMIT_EGF_RESPONSE_120_MCF10A 38 −0.4803 −1.7334 0.009412 0.023187 0.983 6027 tags = 53%, list = 28%, signal = 73% BILD_MYC_ONCOGENIC_SIGNATURE 144 −0.37447 −1.73285 0 0.023232 0.983 4645 tags = 42%, list = 21%, signal = 53% SHEPARD_BMYB_TARGETS 58 −0.43562 −1.73142 0.004762 0.023477 0.983 6032 tags = 57%, list = 28%, signal = 78% REACTOME_AUTODEGRADATION_OF_CDH1_BY_CDH1_(—) 55 −0.44901 −1.72632 0 0.024594 0.988 8446 tags = 64%, list = 39%, APC signal = 103% REACTOME_STABILIZATION_OF_P53 45 −0.45328 −1.72463 0.00232 0.02485 0.988 9592 tags = 76%, list = 44%, signal = 134% NAGASHIMA_NRG1_SIGNALING_UP 151 −0.36805 −1.72373 0 0.024899 0.988 3705 tags = 31%, list = 17%, signal = 37% KANNAN_TP53_TARGETS_DN 15 −0.60828 −1.72134 0.010593 0.025342 0.988 3065 tags = 40%, list = 14%, signal = 46% PAL_PRMT5_TARGETS_UP 183 −0.35915 −1.72133 0 0.025257 0.988 6733 tags = 49%, list = 31%, signal = 70% CHEN_HOXA5_TARGETS_9HR_DN 35 −0.4805 −1.72092 0.002203 0.02525 0.988 5285 tags = 46%, list = 24%, signal = 60% CHEOK_RESPONSE_TO_MERCAPTOPURINE_AND_HD_(—) 21 −0.56181 −1.71985 0.008696 0.025352 0.989 5476 tags = 43%, list = 25%, MTX_DN signal = 57% BHATI_G2M_ARREST_BY_2METHOXYESTRADIOL_UP 92 −0.40056 −1.71724 0.002577 0.025853 0.989 6433 tags = 47%, list = 29%, signal = 66% REACTOME_REPAIR_SYNTHESIS_OF_PATCH_27_30_(—) 15 −0.60537 −1.71296 0.01559 0.026861 0.991 5554 tags = 60%, list = 25%, BASES_LONG_BY_DNA_POLYMERASE signal = 80% REACTOME_RNA_POLYMERASE_I_PROMOTER_ESCAPE 18 −0.56795 −1.70974 0.008909 0.027568 0.993 3988 tags = 44%, list = 18%, signal = 54% KEGG_GALACTOSE_METABOLISM 25 −0.52012 −1.70892 0.00907 0.02767 0.993 4099 tags = 40%, list = 19%, signal = 49% BOYLAN_MULTIPLE_MYELOMA_C_CLUSTER_UP 29 −0.50959 −1.70656 0.008969 0.028226 0.993 2991 tags = 41%, list = 14%, signal = 48% LEE_METASTASIS_AND_RNA_PROCESSING_UP 15 −0.58996 −1.70655 0.022936 0.028129 0.993 8075 tags = 80%, list = 37%, signal = 127% AMIT_SERUM_RESPONSE_480_MCF10A 30 −0.49537 −1.70219 0.009009 0.029016 0.993 3413 tags = 37%, list = 16%, signal = 43% MOOTHA_PGC 307 −0.33049 −1.70183 0 0.029001 0.993 7069 tags = 46%, list = 32%, signal = 67% REACTOME_MRNA_PROCESSING 30 −0.49898 −1.70076 0.002494 0.029224 0.994 8812 tags = 80%, list = 40%, signal = 134% BIOCARTA_DC_PATHWAY 22 −0.5261 −1.6975 0.011876 0.029891 0.994 1999 tags = 32%, list = 9%, signal = 35% WILCOX_PRESPONSE_TO_ROGESTERONE_UP 112 −0.38162 −1.69573 0 0.030222 0.994 5072 tags = 45%, list = 23%, signal = 58% BIOCARTA_P53_PATHWAY 16 −0.57249 −1.69552 0.010707 0.030177 0.994 4124 tags = 56%, list = 19%, signal = 69% DAZARD_RESPONSE_TO_UV_SCC_UP 72 −0.41147 −1.69456 0 0.030338 0.994 3974 tags = 32%, list = 18%, signal = 39% GRAHAM_CML_QUIESCENT_VS_NORMAL_QUIESCENT_(—) 72 −0.40487 −1.69363 0 0.030502 0.994 6001 tags = 57%, list = 27%, UP signal = 78% LANDIS_ERBB2_BREAST_TUMORS_324_UP 139 −0.36646 −1.69319 0 0.030545 0.994 4710 tags = 34%, list = 22%, signal = 43% CHIARADONNA_NEOPLASTIC_TRANSFORMATION_(—) 119 −0.37042 −1.69273 0 0.030552 0.994 5970 tags = 45%, list = 27%, KRAS_UP signal = 62% KEGG_ONE_CARBON_POOL_BY_FOLATE 15 −0.59992 −1.69119 0.018947 0.030866 0.996 4791 tags = 73%, list = 22%, signal = 94% DOUGLAS_BMI1_TARGETS_UP 442 −0.31592 −1.68759 0 0.031609 0.996 4215 tags = 29%, list = 19%, signal = 35% OLSSON_E2F3_TARGETS_DN 22 −0.53086 −1.68742 0.011737 0.03154 0.996 4086 tags = 50%, list = 19%, signal = 61% WILLIAMS_ESR1_TARGETS_UP 19 −0.55372 −1.68326 0.010504 0.032535 0.999 4662 tags = 47%, list = 21%, signal = 60% PENG_LEUCINE_DEPRIVATION_DN 41 −0.45777 −1.681 0.009153 0.033002 0.999 8257 tags = 68%, list = 38%, signal = 109% KEGG_FC_EPSILON_RI_SIGNALING_PATHWAY 76 −0.40196 −1.68074 0.002577 0.03295 0.999 1999 tags = 14%, list = 9%, signal = 16% RHODES_CANCER_META_SIGNATURE 52 −0.43623 −1.67879 0.004926 0.033501 0.999 8353 tags = 65%, list = 38%, signal = 105% BROWNE_HCMV_INFECTION_14HR_UP 123 −0.36371 −1.67858 0 0.033458 0.999 6904 tags = 49%, list = 32%, signal = 71% SPIELMAN_LYMPHOBLAST_EUROPEAN_VS_ASIAN_UP 406 −0.3221 −1.6748 0 0.034351 0.999 6365 tags = 38%, list = 29%, signal = 53% DIRMEIER_LMP1_RESPONSE_EARLY 49 −0.43597 −1.67219 0.00241 0.0349 0.999 5795 tags = 43%, list = 26%, signal = 58% KEGG_CYTOKINE_CYTOKINE_RECEPTOR_INTERACTION 202 −0.34329 −1.67194 0 0.034846 0.999 3494 tags = 29%, list = 16%, signal = 34% BOYAULT_LIVER_CANCER_SUBCLASS_G12_UP 35 −0.47501 −1.67121 0.011628 0.034991 0.999 3831 tags = 37%, list = 18%, signal = 45% REACTOME_PREFOLDIN_MEDIATED_TRANSFER_OF_(—) 21 −0.53257 −1.66687 0.013857 0.036009 0.999 7425 tags = 67%, list = 34%, SUBSTRATE_TO_CCT_TRIC signal = 101% GINESTIER_BREAST_CANCER_ZNF217_AMPLIFIED_DN 226 −0.33501 −1.66503 0 0.036448 0.999 6641 tags = 39%, list = 30%, signal = 55% REACTOME_EGFR_DOWNREGULATION 23 −0.51833 −1.66296 0.020548 0.036971 0.999 5650 tags = 35%, list = 26%, signal = 47% REACTOME_PYRIMIDINE_METABOLISM 20 −0.53158 −1.66003 0.013274 0.037713 0.999 1826 tags = 40%, list = 8%, signal = 44% VANTVEER_BREAST_CANCER_BRCA1_UP 25 −0.51733 −1.65758 0.019313 0.038342 0.999 5293 tags = 44%, list = 24%, signal = 58% KEGG_GLYCINE_SERINE_AND_THREONINE_METABOLISM 25 −0.52385 −1.65415 0.017021 0.039205 1 3223 tags = 40%, list = 15%, signal = 47% CHAUHAN_RESPONSE_TO_METHOXYESTRADIOL_UP 44 −0.4478 −1.65346 0.009174 0.03929 1 7597 tags = 66%, list = 35%, signal = 101% ACEVEDO_LIVER_CANCER_WITH_H3K9ME3_DN 57 −0.41475 −1.65304 0 0.039293 1 5071 tags = 44%, list = 23%, signal = 57% PARENT_MTOR_SIGNALING_DN 34 −0.4655 −1.65233 0.018265 0.039453 1 3138 tags = 32%, list = 14%, signal = 38% ACEVEDO_NORMAL_TISSUE_ADJACENT_TO_LIVER_(—) 278 −0.32185 −1.65157 0 0.03953 1 5186 tags = 31%, list = 24%, TUMOR_DN signal = 40% AMUNDSON_GENOTOXIC_SIGNATURE 76 −0.39026 −1.64944 0.002632 0.040202 1 2400 tags = 26%, list = 11%, signal = 29% WANG_METHYLATED_IN_BREAST_CANCER 28 −0.48962 −1.64877 0.004556 0.040307 1 5766 tags = 50%, list = 26%, signal = 68% SHEPARD_CRUSH_AND_BURN_MUTANT_DN 138 −0.36039 −1.64233 0 0.042291 1 6287 tags = 46%, list = 29%, signal = 65% TONKS_TARGETS_OF_RUNX1_RUNX1T1_FUSION_(—) 160 −0.34785 −1.64217 0 0.042209 1 5564 tags = 44%, list = 25%, MONOCYTE_UP signal = 58% SMIRNOV_CIRCULATING_ENDOTHELIOCYTES_IN_(—) 134 −0.35747 −1.64134 0 0.042323 1 1881 tags = 22%, list = 9%, CANCER_UP signal = 24% GEORGES_CELL_CYCLE_MIR192_TARGETS 55 −0.41585 −1.63727 0.009009 0.043643 1 6178 tags = 51%, list = 28%, signal = 71% VANHARANTA_UTERINE_FIBROID_WITH_7Q_DELETION_UP 55 −0.42177 −1.63642 0.005464 0.043819 1 8221 tags = 60%, list = 38%, signal = 96% DACOSTA_UV_RESPONSE_VIA_ERCC3_UP 263 −0.327 −1.63636 0 0.043695 1 6170 tags = 39%, list = 28%, signal = 54% REACTOME_GLOBAL_GENOMIC_NER 33 −0.46089 −1.63605 0.01171 0.043666 1 5837 tags = 55%, list = 27%, signal = 74% REACTOME_SYNTHESIS_OF_GPI_ANCHORED_PROTEINS 23 −0.50984 −1.63599 0.015556 0.043558 1 5332 tags = 39%, list = 24%, signal = 52% KEGG_PORPHYRIN_AND_CHLOROPHYLL_METABOLISM 23 −0.50638 −1.63489 0.013793 0.043736 1 2880 tags = 39%, list = 13%, signal = 45% TURASHVILI_BREAST_NORMAL_DUCTAL_VS_LOBULAR_(—) 43 −0.44105 −1.63472 0.002347 0.043678 1 4159 tags = 30%, list = 19%, UP signal = 37% HSC_MATURE_FETAL 21 −0.52771 −1.63326 0.020548 0.044137 1 6006 tags = 57%, list = 27%, signal = 79% STEIN_ESRRA_TARGETS_RESPONSIVE_TO_ESTROGEN_(—) 21 −0.51886 −1.63258 0.027957 0.044203 1 1226 tags = 33%, list = 6%, UP signal = 35% SHEPARD_CRUSH_AND_BURN_MUTANT_UP 125 −0.35859 −1.62825 0.002755 0.045705 1 4532 tags = 39%, list = 21%, signal = 49% REACTOME_METABOLISM_OF_VITAMINS_AND_(—) 40 −0.44337 −1.62546 0.016129 0.046522 1 3969 tags = 40%, list = 18%, COFACTORS signal = 49% VANTVEER_BREAST_CANCER_ESR1_DN 176 −0.33964 −1.62501 0.00277 0.046595 1 4524 tags = 31%, list = 21%, signal = 38% REACTOME_METABLISM_OF_NUCLEOTIDES 64 −0.40412 −1.62145 0 0.047924 1 4372 tags = 42%, list = 20%, signal = 53% SUNG_METASTASIS_STROMA_UP 89 −0.37528 −1.62073 0.007895 0.048055 1 5198 tags = 43%, list = 24%, signal = 56% WEIGEL_OXIDATIVE_STRESS_BY_HNE_AND_H2O2 34 −0.44773 −1.61991 0.009524 0.048239 1 5259 tags = 32%, list = 24%, signal = 43% BIOCARTA_PROTEASOME_PATHWAY 18 −0.54104 −1.61938 0.019523 0.048296 1 9592 tags = 83%, list = 44%, signal = 148% KEGG_AMINO_SUGAR_AND_NUCLEOTIDE_SUGAR_(—) 41 −0.44482 −1.61843 0.015038 0.048492 1 4255 tags = 37%, list = 19%, METABOLISM signal = 45% PELLICCIOTTA_HDAC_IN_ANTIGEN_PRESENTATION_(—) 57 −0.40746 −1.61747 0.004751 0.048706 1 8257 tags = 53%, list = 38%, UP signal = 84% LANDIS_ERBB2_BREAST_PRENEOPLASTIC_UP 21 −0.52713 −1.61628 0.03304 0.049018 1 5507 tags = 48%, list = 25%, signal = 64% SHEPARD_BMYB_MORPHOLINO_DN 151 −0.34543 −1.61546 0 0.04917 1 4797 tags = 38%, list = 22%, signal = 49% YEGNASUBRAMANIAN_PROSTATE_CANCER 91 −0.3681 −1.61505 0.00241 0.049198 1 5394 tags = 38%, list = 25%, signal = 51% KIM_WT1_TARGETS_UP 183 −0.34191 −1.61475 0 0.049181 1 4812 tags = 33%, list = 22%, signal = 42% MOHANKUMAR_TLX1_TARGETS_UP 325 −0.31306 −1.61407 0 0.049308 1 5689 tags = 37%, list = 26%, signal = 49% AMUNDSON_RESPONSE_TO_ARSENITE 159 −0.34303 −1.61281 0 0.049661 1 5229 tags = 31%, list = 24%, signal = 41% KEGG_PANTOTHENATE_AND_COA_BIOSYNTHESIS 15 −0.55962 −1.61174 0.034014 0.049863 1 1891 tags = 27%, list = 9%, signal = 29% KEGG_P53_SIGNALING_PATHWAY 61 −0.40197 −1.60772 0.002494 0.051363 1 5516 tags = 46%, list = 25%, signal = 61% RIZ_ERYTHROID_DIFFERENTIATION_CCNE1 38 −0.44707 −1.60742 0.016827 0.051366 1 4135 tags = 39%, list = 19%, signal = 49% HAHTOLA_MYCOSIS_FUNGOIDES_CD4_UP 52 −0.41002 −1.60651 0.00907 0.051599 1 2819 tags = 27%, list = 13%, signal = 31% MAHAJAN_RESPONSE_TO_IL1A_DN 53 −0.41564 −1.60627 0.006834 0.051554 1 4977 tags = 34%, list = 23%, signal = 44% KORKOLA_EMBRYONIC_CARCINOMA_VS_SEMINOMA_(—) 19 −0.52884 −1.60556 0.017131 0.051738 1 2193 tags = 37%, list = 10%, UP signal = 41% REACTOME_RNA_POLYMERASE_III_TRANSCRIPTION 32 −0.45961 −1.60364 0.013986 0.052373 1 6005 tags = 66%, list = 27%, signal = 90% KEGG_RNA_DEGRADATION 50 −0.42032 −1.60343 0.009153 0.052308 1 7202 tags = 64%, list = 33%, signal = 95% CHEN_HOXA5_TARGETS_9HR_UP 157 −0.33909 −1.60172 0 0.052912 1 6240 tags = 38%, list = 29%, signal = 53% NAKAMURA_METASTASIS 35 −0.45954 −1.60126 0.014563 0.052967 1 4215 tags = 34%, list = 19%, signal = 42% MORI_MATURE_B_LYMPHOCYTE_DN 56 −0.41156 −1.60091 0.00905 0.052991 1 4737 tags = 41%, list = 22%, signal = 52% REACTOME_METABOLISM_OF_MRNA 42 −0.43055 −1.60047 0.009132 0.053032 1 7211 tags = 60%, list = 33%, signal = 89% KEGG_N_GLYCAN_BIOSYNTHESIS 40 −0.4325 −1.59985 0.015801 0.053124 1 6311 tags = 50%, list = 29%, signal = 70% JEON_SMAD6_TARGETS_DN 18 −0.54236 −1.59558 0.026786 0.054948 1 5348 tags = 50%, list = 24%, signal = 66% CLASPER_LYMPHATIC_VESSELS_DURING_METASTASIS_(—) 17 −0.55069 −1.59427 0.030568 0.055381 1 2913 tags = 41%, list = 13%, UP signal = 47% AMIT_EGF_RESPONSE_480_HELA 136 −0.34576 −1.59203 0.002591 0.056209 1 3870 tags = 29%, list = 18%, signal = 36% THEILGAARD_NEUTROPHIL_AT_SKIN_WOUND_UP 65 −0.38845 −1.59076 0.004762 0.056647 1 5493 tags = 37%, list = 25%, signal = 49% MILI_PSEUDOPODIA_HAPTOTAXIS_UP 438 −0.29623 −1.58848 0 0.057541 1 6731 tags = 38%, list = 31%, signal = 54% KEGG_SELENOAMINO_ACID_METABOLISM 20 −0.52272 −1.5861 0.026144 0.058513 1 7217 tags = 65%, list = 33%, signal = 97% KORKOLA_EMBRYONAL_CARCINOMA_UP 36 −0.44176 −1.58582 0.011601 0.058493 1 6328 tags = 47%, list = 29%, signal = 66% FONTAINE_FOLLICULAR_THYROID_ADENOMA_UP 57 −0.40056 −1.58505 0.015345 0.058613 1 3065 tags = 30%, list = 14%, signal = 35% RIZ_ERYTHROID_DIFFERENTIATION 71 −0.38675 −1.58081 0.009592 0.060491 1 4993 tags = 37%, list = 23%, signal = 47% REACTOME_PYRUVATE_METABOLISM_AND_TCA_(—) 32 −0.44675 −1.57427 0.021378 0.06352 1 7132 tags = 53%, list = 33%, CYCLE signal = 79% WANG_RESPONSE_TO_ANDROGEN_UP 23 −0.48805 −1.57297 0.024943 0.063962 1 6045 tags = 61%, list = 28%, signal = 84% KEGG_STEROID_BIOSYNTHESIS 16 −0.54002 −1.57091 0.027254 0.064832 1 5329 tags = 56%, list = 24%, signal = 74% JAEGER_METASTASIS_UP 37 −0.43504 −1.57013 0.01087 0.065086 1 3001 tags = 30%, list = 14%, signal = 34% LEONARD_HYPOXIA 29 −0.46322 −1.56924 0.017699 0.065355 1 2233 tags = 28%, list = 10%, signal = 31% STEIN_ESRRA_TARGETS 401 −0.29457 −1.56577 0 0.066972 1 5116 tags = 30%, list = 23%, signal = 39% JIANG_TIP30_TARGETS_DN 23 −0.49545 −1.56502 0.028889 0.067216 1 5302 tags = 52%, list = 24%, signal = 69% KEGG_AUTOIMMUNE_THYROID_DISEASE 23 −0.49272 −1.56463 0.030905 0.06723 1 1694 tags = 30%, list = 8%, signal = 33% BIOCARTA_INTEGRIN_PATHWAY 38 −0.42913 −1.56369 0.014354 0.06759 1 5869 tags = 32%, list = 27%, signal = 43% CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_2 255 −0.30936 −1.56175 0 0.06838 1 4105 tags = 28%, list = 19%, signal = 34% HEDENFALK_BREAST_CANCER_BRCA1_VS_BRCA2 25 −0.47245 −1.55993 0.033097 0.069118 1 3574 tags = 40%, list = 16%, signal = 48% MAHADEVAN_IMATINIB_RESISTANCE_UP 16 −0.54102 −1.55993 0.042827 0.068943 1 3130 tags = 38%, list = 14%, signal = 44% MUELLER_METHYLATED_IN_GLIOBLASTOMA 30 −0.45712 −1.5577 0.020737 0.069831 1 3426 tags = 40%, list = 16%, signal = 47% BOYAULT_LIVER_CANCER_SUBCLASS_G23_UP 42 −0.42862 −1.5574 0.011601 0.069814 1 6673 tags = 60%, list = 30%, signal = 85% REACTOME_RNA_POLYMERASE_I_PROMOTER_CLEARANCE 33 −0.43867 −1.55657 0.021505 0.070054 1 3988 tags = 36%, list = 18%, signal = 44% BIOCARTA_MCM_PATHWAY 18 −0.51775 −1.55555 0.030043 0.070423 1 7652 tags = 89%, list = 35%, signal = 137% CASTELLANO_NRAS_TARGETS_UP 66 −0.37914 −1.55523 0.009662 0.070421 1 1258 tags = 15%, list = 6%, signal = 16% BILD_E2F3_ONCOGENIC_SIGNATURE 172 −0.32638 −1.55522 0 0.070248 1 3202 tags = 24%, list = 15%, signal = 28% WEINMANN_ADAPTATION_TO_HYPOXIA_DN 32 −0.43747 −1.55424 0.032407 0.070646 1 2418 tags = 38%, list = 11%, signal = 42% KAPOSI_LIVER_CANCER_POOR_SURVIVAL_UP 16 −0.54639 −1.55257 0.043573 0.071408 1 4016 tags = 31%, list = 18%, signal = 38% PASQUALUCCI_LYMPHOMA_BY_GC_STAGE_UP 246 −0.31478 −1.55237 0 0.071317 1 3587 tags = 26%, list = 16%, signal = 30% REACTOME_POST_TRANSLATIONAL_PROTEIN_(—) 37 −0.43412 −1.55172 0.017279 0.071446 1 6520 tags = 46%, list = 30%, MODIFICATION signal = 65% CAFFAREL_RESPONSE_TO_THC_DN 21 −0.50052 −1.5485 0.030702 0.073139 1 5819 tags = 52%, list = 27%, signal = 71% REACTOME_G2_M_TRANSITION 71 −0.36948 −1.5485 0.013123 0.072959 1 8210 tags = 52%, list = 38%, signal = 83% GAJATE_RESPONSE_TO_TRABECTEDIN_DN 15 −0.53965 −1.54414 0.046709 0.075117 1 7028 tags = 67%, list = 32%, signal = 98% STEIN_ESRRA_TARGETS_UP 298 −0.3001 −1.54387 0 0.075021 1 4541 tags = 27%, list = 21%, signal = 33% MOOTHA_VOXPHOS 79 −0.37294 −1.54361 0.009975 0.074979 1 9439 tags = 54%, list = 43%, signal = 95% SWEET_KRAS_TARGETS_UP 17 −0.52812 −1.5415 0.03397 0.075917 1 3664 tags = 29%, list = 17%, signal = 35% KERLEY_RESPONSE_TO_CISPLATIN_UP 35 −0.43382 −1.53987 0.021028 0.076598 1 1839 tags = 29%, list = 8%, signal = 31% WINTER_HYPOXIA_UP 70 −0.37486 −1.5381 0.012658 0.077262 1 2904 tags = 29%, list = 13%, signal = 33% HELLER_HDAC_TARGETS_DN 222 −0.30689 −1.53637 0 0.077987 1 2837 tags = 22%, list = 13%, signal = 25% NAKAMURA_METASTASIS_MODEL_UP 32 −0.43733 −1.5362 0.021786 0.077897 1 3784 tags = 31%, list = 17%, signal = 38% TSENG_IRS1_TARGETS_UP 110 −0.3502 −1.53609 0.00542 0.077758 1 5390 tags = 42%, list = 25%, signal = 55% SAGIV_CD24_TARGETS_DN 36 −0.42214 −1.53213 0.014706 0.079849 1 2265 tags = 25%, list = 10%, signal = 28% ONDER_CDH1_TARGETS_1_DN 127 −0.33147 −1.53188 0.005249 0.079797 1 4540 tags = 31%, list = 21%, signal = 40% REACTOME_RNA_POLYMERASE_I_CHAIN_ELONGATION 21 −0.50165 −1.53108 0.041394 0.080008 1 8169 tags = 62%, list = 37%, signal = 99% SLEBOS_HEAD_AND_NECK_CANCER_WITH_HPV_UP 59 −0.38344 −1.53046 0.009732 0.080164 1 6770 tags = 54%, list = 31%, signal = 78% GENTILE_UV_LOW_DOSE_DN 17 −0.50817 −1.52488 0.054622 0.083273 1 3800 tags = 47%, list = 17%, signal = 57% DACOSTA_UV_RESPONSE_VIA_ERCC3_COMMON_UP 48 −0.40433 −1.52453 0.030952 0.08328 1 3115 tags = 29%, list = 14%, signal = 34% GUTIERREZ_MULTIPLE_MYELOMA_DN 29 −0.44814 −1.52383 0.025806 0.083507 1 6150 tags = 52%, list = 28%, signal = 72% NAKAMURA_TUMOR_ZONE_PERIPHERAL_VS_CENTRAL_(—) 209 −0.31195 −1.52226 0 0.084241 1 6207 tags = 41%, list = 28%, UP signal = 57% GENTILE_UV_LOW_DOSE_UP 17 −0.50817 −1.5203 0.045977 0.085253 1 3800 tags = 47%, list = 17%, signal = 57% KEGG_MELANOMA 70 −0.37406 −1.51908 0.020202 0.085739 1 3471 tags = 21%, list = 16%, signal = 25% GAZDA_DIAMOND_BLACKFAN_ANEMIA_PROGENITOR_(—) 48 −0.39891 −1.51767 0.011547 0.086379 1 7491 tags = 65%, list = 34%, DN signal = 98% HEDENFALK_BREAST_CANCER_BRACX_UP 15 −0.53281 −1.51618 0.04186 0.087139 1 4411 tags = 33%, list = 20%, signal = 42% PYEON_CANCER_HEAD_AND_NECK_VS_CERVICAL_UP 129 −0.32837 −1.51464 0.002833 0.087896 1 5555 tags = 40%, list = 25%, signal = 54% BOHN_PRIMARY_IMMUNODEFICIENCY_SYNDROM_UP 30 −0.44959 −1.5146 0.035088 0.087709 1 6557 tags = 60%, list = 30%, signal = 86% KEGG_PRION_DISEASES 31 −0.43419 −1.50972 0.029724 0.090708 1 3648 tags = 29%, list = 17%, signal = 35% SHAFFER_IRF4_TARGETS_IN_ACTIVATED_DENDRITIC_(—) 59 −0.37847 −1.50914 0.010127 0.090858 1 3877 tags = 34%, list = 18%, CELL signal = 41% REACTOME_FRS2MEDIATED_CASCADE 26 −0.45398 −1.50573 0.034884 0.092953 1 2299 tags = 27%, list = 11%, signal = 30% REACTOME_METABOLISM_OF_PROTEINS 168 −0.31495 −1.50419 0.00271 0.093745 1 7289 tags = 32%, list = 33%, signal = 47% SENESE_HDAC3_TARGETS_DN 380 −0.28679 −1.50414 0 0.09355 1 4912 tags = 31%, list = 22%, signal = 39% SHAFFER_IRF4_TARGETS_IN_MYELOMA_VS_MATURE_(—) 92 −0.34437 −1.50159 0.002457 0.094919 1 6045 tags = 42%, list = 28%, B_LYMPHOCYTE signal = 58% VANTVEER_BREAST_CANCER_METASTASIS_DN 87 −0.34766 −1.5009 0.005277 0.095133 1 6885 tags = 47%, list = 31%, signal = 68% BROWNE_HCMV_INFECTION_18HR_UP 150 −0.32006 −1.5001 0 0.095376 1 5934 tags = 39%, list = 27%, signal = 53% CHO_NR4A1_TARGETS 21 −0.48094 −1.4997 0.03908 0.095394 1 2408 tags = 24%, list = 11%, signal = 27% LANDIS_ERBB2_BREAST_TUMORS_65_UP 21 −0.47553 −1.49725 0.041943 0.096736 1 180 tags = 14%, list = 1%, signal = 14% SUNG_METASTASIS_STROMA_DN 37 −0.42164 −1.49584 0.033019 0.097521 1 4568 tags = 46%, list = 21%, signal = 58% KEGG_GLIOMA 60 −0.37437 −1.49578 0.028986 0.097335 1 3471 tags = 22%, list = 16%, signal = 26% LOCKWOOD_AMPLIFIED_IN_LUNG_CANCER 146 −0.32124 −1.49433 0.005181 0.098139 1 8242 tags = 52%, list = 38%, signal = 83% SANA_RESPONSE_TO_IFNG_DN 69 −0.3646 −1.49259 0.012077 0.099073 1 6606 tags = 46%, list = 30%, signal = 66% GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_(—) 15 −0.54264 −1.49204 0.044681 0.09925 1 4810 tags = 60%, list = 22%, RED_UP signal = 77% WONG_PROTEASOME_GENE_MODULE 45 −0.39346 −1.49194 0.023981 0.099068 1 6478 tags = 44%, list = 30%, signal = 63% REACTOME_SIGNALLING_TO_RAS 25 −0.45679 −1.49192 0.027778 0.098842 1 5189 tags = 28%, list = 24%, signal = 37% HOFFMANN_PRE_BI_TO_LARGE_PRE_(—) 18 −0.4987 −1.49113 0.04157 0.099205 1 3181 tags = 44%, list = 15%, BII_LYMPHOCYTE_UP signal = 52% KOKKINAKIS_METHIONINE_DEPRIVATION_96HR_DN 68 −0.35949 −1.48846 0.006928 0.100901 1 4780 tags = 32%, list = 22%, signal = 41% FLECHNER_BIOPSY_KIDNEY_TRANSPLANT_ OK_VS_(—) 20 −0.48691 −1.48792 0.058275 0.101095 1 3648 tags = 45%, list = 17%, DONOR_DN signal = 54% FULCHER_INFLAMMATORY_RESPONSE_ LECTIN_VS_(—) 425 −0.27997 −1.48736 0 0.101318 1 4807 tags = 31%, list = 22%, LPS_UP signal = 39% ALONSO_METASTASIS_UP 139 −0.3209 −1.48195 0 0.10495 1 6027 tags = 37%, list = 28%, signal = 51% SEKI_INFLAMMATORY_RESPONSE_LPS_UP 75 −0.35431 −1.4819 0.015584 0.104744 1 2819 tags = 25%, list = 13%, signal = 29% ROZANOV_MMP14_TARGETS_SUBSET 31 −0.43222 −1.48066 0.03125 0.105382 1 3313 tags = 35%, list = 15%, signal = 42% LIU_TARGETS_OF_VMYB_VS_CMYB_DN 36 −0.42063 −1.48011 0.039312 0.105606 1 1816 tags = 28%, list = 8%, signal = 30% YAO_TEMPORAL_RESPONSE_ TO_PROGESTERONE_(—) 28 −0.44457 −1.48001 0.045662 0.105435 1 1428 tags = 21%, list = 7%, CLUSTER_5 signal = 23% NAM_FXYD5_TARGETS_DN 15 −0.51417 −1.47977 0.051282 0.105388 1 6150 tags = 53%, list = 28%, signal = 74% HAMAI_APOPTOSIS_VIA_TRAIL_DN 110 −0.33103 −1.47919 0.005376 0.105494 1 4416 tags = 29%, list = 20%, signal = 36% ZHOU_INFLAMMATORY_RESPONSE_LIVE_UP 337 −0.28625 −1.47794 0 0.106193 1 4884 tags = 31%, list = 22%, signal = 39% ENK_UV_RESPONSE_EPIDERMIS_UP 247 −0.29261 −1.47656 0 0.107043 1 4059 tags = 30%, list = 19%, signal = 36% JAERVINEN_AMPLIFIED_IN_LARYNGEAL_CANCER 31 −0.43216 −1.47452 0.038278 0.108221 1 4458 tags = 42%, list = 20%, signal = 53% REACTOME_METABOLISM_OF_CARBOHYDRATES 107 −0.3253 −1.47395 0.002584 0.108405 1 6272 tags = 43%, list = 29%, signal = 60% REACTOME_RNA_POLYMERASE_I_TRANSCRIPTION_(—) 19 −0.49033 −1.47272 0.037209 0.109075 1 5229 tags = 42%, list = 24%, TERMINATION signal = 55% BIOCARTA_NKT_PATHWAY 27 −0.45331 −1.47259 0.046296 0.108961 1 1001 tags = 26%, list = 5%, signal = 27% CHIN_BREAST_CANCER_COPY_NUMBER_UP 19 −0.48619 −1.46993 0.056277 0.110731 1 4901 tags = 47%, list = 22%, signal = 61% BHATI_G2M_ARREST_BY_2METHOXYESTRADIOL_DN 93 −0.33428 −1.46694 0.010959 0.112645 1 5711 tags = 38%, list = 26%, signal = 51% KEGG_PURINE_METABOLISM 144 −0.31203 −1.46666 0.00271 0.112641 1 6525 tags = 46%, list = 30%, signal = 65% KEGG_CYSTEINE_AND_METHIONINE_METABOLISM 30 −0.43055 −1.46474 0.041284 0.113858 1 4170 tags = 33%, list = 19%, signal = 41% KORKOLA_YOLK_SAC_TUMOR_UP 16 −0.49958 −1.46269 0.05977 0.115226 1 7367 tags = 50%, list = 34%, signal = 75% SCHLOSSER_SERUM_RESPONSE_AUGMENTED_BY_MYC 89 −0.33937 −1.46002 0.016043 0.116993 1 8503 tags = 63%, list = 39%, signal = 102% BIOCARTA_P53HYPOXIA_PATHWAY 21 −0.4684 −1.45891 0.05794 0.117743 1 4235 tags = 43%, list = 19%, signal = 53% NUNODA_RESPONSE_TO_DASATINIB_IMATINIB_UP 28 −0.43895 −1.45731 0.060046 0.118697 1 3952 tags = 39%, list = 18%, signal = 48% LEE_LIVER_CANCER_SURVIVAL_DN 105 −0.33219 −1.45577 0.010811 0.119604 1 7770 tags = 49%, list = 35%, signal = 75% SHAFFER_IRF4_TARGETS_IN_PLASMA_CELL_VS_MATURE_(—) 62 −0.36088 −1.45474 0.021635 0.120228 1 4008 tags = 31%, list = 18%, B_LYMPHOCYTE signal = 37% PYEON_HPV_POSITIVE_TUMORS_UP 58 −0.36375 −1.45304 0.026005 0.121441 1 6468 tags = 48%, list = 30%, signal = 68% LINDGREN_BLADDER_CANCER_WITH_LOH_IN_CHR9Q 87 −0.33999 −1.45283 0.009732 0.121316 1 7167 tags = 49%, list = 33%, signal = 73% ENK_UV_RESPONSE_KERATINOCYTE_UP 442 −0.27461 −1.45076 0 0.122851 1 6664 tags = 36%, list = 30%, signal = 50% MCCLUNG_DELTA_FOSB_TARGETS_2WK 43 −0.39175 −1.4494 0.042056 0.123754 1 4790 tags = 37%, list = 22%, signal = 48% VARELA_ZMPSTE24_TARGETS_UP 38 −0.39554 −1.44606 0.033493 0.126183 1 3737 tags = 37%, list = 17%, signal = 44% ZHAN_MULTIPLE_MYELOMA_MS_UP 34 −0.41283 −1.44598 0.04119 0.125977 1 836 tags = 18%, list = 4%, signal = 18% ZUCCHI_METASTASIS_DN 21 −0.45835 −1.44406 0.056948 0.127368 1 3297 tags = 29%, list = 15%, signal = 34% TOOKER_GEMCITABINE_RESISTANCE_DN 108 −0.32502 −1.44285 0.01897 0.128182 1 5342 tags = 41%, list = 24%, signal = 54% WEIGEL_OXIDATIVE_STRESS_RESPONSE 25 −0.44035 −1.44226 0.061834 0.128403 1 6203 tags = 48%, list = 28%, signal = 67% REACTOME_MRNA_SPLICING_MINOR_PATHWAY 36 −0.40293 −1.44226 0.035 0.128133 1 8812 tags = 72%, list = 40%, signal = 121% SCIAN_INVERSED_TARGETS_OF_TP53_AND_TP73_DN 24 −0.44228 −1.43996 0.050847 0.129878 1 2384 tags = 25%, list = 11%, signal = 28% YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_(—) 62 −0.35741 −1.43816 0.039216 0.13116 1 8291 tags = 58%, list = 38%, CLUSTER_10 signal = 93% GESERICK_TERT_TARGETS_DN 19 −0.46809 −1.43387 0.063877 0.134421 1 5445 tags = 58%, list = 25%, signal = 77% SYED_ESTRADIOL_RESPONSE 15 −0.50256 −1.43354 0.075688 0.134435 1 1119 tags = 27%, list = 5%, signal = 28% REACTOME_CITRIC_ACID_CYCLE 18 −0.48351 −1.43321 0.072072 0.134449 1 9447 tags = 78%, list = 43%, signal = 137% GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_(—) 19 −0.46937 −1.43264 0.072893 0.134647 1 5056 tags = 47%, list = 23%, MAGENTA_UP signal = 62% CAFFAREL_RESPONSE_TO_THC_24HR_5_UP 23 −0.44394 −1.43258 0.067834 0.134415 1 6027 tags = 48%, list = 28%, signal = 66% TOOKER_RESPONSE_TO_BEXAROTENE_UP 108 −0.32502 −1.4324 0.017413 0.134261 1 5342 tags = 41%, list = 24%, signal = 54% NIKOLSKY_BREAST_CANCER_17Q11_Q21_AMPLICON 74 −0.34376 −1.43141 0.029851 0.134823 1 4558 tags = 32%, list = 21%, signal = 41% DACOSTA_UV_RESPONSE_VIA_ERCC3_XPCS_UP 15 −0.49893 −1.42982 0.079523 0.136028 1 2092 tags = 20%, list = 10%, signal = 22% ZHOU_INFLAMMATORY_RESPONSE_FIMA_UP 363 −0.27303 −1.4289 0 0.136663 1 4767 tags = 28%, list = 22%, signal = 36% FONTAINE_PAPILLARY_THYROID_CARCINOMA_DN 61 −0.35621 −1.42837 0.039443 0.136889 1 3080 tags = 25%, list = 14%, signal = 29% REACTOME_E2F_TRANSCRIPTIONAL_TARGETS_AT_G1_S 19 −0.47601 −1.42739 0.053991 0.137516 1 3495 tags = 47%, list = 16%, signal = 56% LUND_SILENCED_BY_METHYLATION 15 −0.49663 −1.42579 0.081678 0.138766 1 3242 tags = 27%, list = 15%, signal = 31% WANG_RESPONSE_TO_FORSKOLIN_UP 17 −0.48715 −1.42558 0.071111 0.138668 1 6045 tags = 59%, list = 28%, signal = 81% SESTO_RESPONSE_TO_UV_C4 17 −0.47406 −1.42534 0.088167 0.138601 1 6342 tags = 65%, list = 29%, signal = 91% STARK_PREFRONTAL_CORTEX_22Q11_DELETION_DN 438 −0.27075 −1.42474 0 0.138849 1 6692 tags = 36%, list = 31%, signal = 51% BHATTACHARYA_EMBRYONIC_STEM_CELL 62 −0.35682 −1.42423 0.040189 0.138977 1 2402 tags = 24%, list = 11%, signal = 27% BIOCARTA_SHH_PATHWAY 15 −0.4984 −1.42376 0.077778 0.139189 1 1205 tags = 27%, list = 6%, signal = 28% REACTOME_CONVERSION_FROM_APC_CDC20_TO_ APC_(—) 16 −0.48592 −1.4233 0.087527 0.139328 1 7138 tags = 56%, list = 33%, CDH1_IN_LATE_ANAPHASE signal = 83% RICKMAN_TUMOR_DIFFERENTIATED_WELL_VS_POORLY_(—) 269 −0.2814 −1.42256 0.003311 0.139667 1 2935 tags = 19%, list = 13%, DN signal = 22% ABE_VEGFA_TARGETS_2HR 16 −0.49199 −1.42146 0.078125 0.14043 1 3857 tags = 31%, list = 18%, signal = 38% MULLIGHAN_MLL_SIGNATURE_1_DN 190 −0.2899 −1.41882 0.002933 0.142577 1 3575 tags = 25%, list = 16%, signal = 29% NIKOLSKY_BREAST_CANCER_11Q12_Q14_AMPLICON 116 −0.31321 −1.41616 0.014205 0.144815 1 5767 tags = 38%, list = 26%, signal = 51% RICKMAN_HEAD_AND_NECK_CANCER_D 21 −0.46169 −1.41475 0.077803 0.145862 1 2856 tags = 33%, list = 13%, signal = 38% HELLER_SILENCED_BY_METHYLATION_DN 82 −0.32818 −1.41447 0.040865 0.145871 1 3138 tags = 24%, list = 14%, signal = 28% REACTOME_LOSS_OF_NLP_FROM_MITOTIC_CENTROSOMES 52 −0.36399 −1.41391 0.045564 0.146124 1 7600 tags = 44%, list = 35%, signal = 68% GAUSSMANN_MLL_AF4_FUSION_TARGETS_D_UP 29 −0.4174 −1.41092 0.06422 0.148574 1 125 tags = 10%, list = 1%, signal = 10% LIAO_HAVE_SOX4_BINDING_SITES 34 −0.39227 −1.40797 0.050239 0.151067 1 3422 tags = 29%, list = 16%, signal = 35% REACTOME_G1_PHASE 15 −0.49867 −1.40719 0.067982 0.151451 1 5167 tags = 47%, list = 24%, signal = 61% KEGG_HUNTINGTONS_DISEASE 151 −0.29949 −1.40388 0.019126 0.15437 1 9317 tags = 54%, list = 43%, signal = 94% DUTTA_APOPTOSIS_VIA_NFKB 27 −0.42005 −1.40305 0.067146 0.154958 1 5445 tags = 44%, list = 25%, signal = 59% ZHANG_ANTIVIRAL_RESPONSE_TO_RIBAVIRIN_DN 38 −0.38083 −1.40241 0.062053 0.155326 1 611 tags = 13%, list = 3%, signal = 14% CHUNG_BLISTER_CYTOTOXICITY_UP 103 −0.31972 −1.40192 0.023316 0.155473 1 6392 tags = 48%, list = 29%, signal = 67% STREICHER_LSM1_TARGETS_DN 16 −0.47911 −1.40091 0.081818 0.156243 1 3808 tags = 44%, list = 17%, signal = 53% GAL_LEUKEMIC_STEM_CELL_DN 179 −0.28739 −1.39983 0.006042 0.156978 1 5413 tags = 37%, list = 25%, signal = 49% KANG_CISPLATIN_RESISTANCE_UP 15 −0.48395 −1.39942 0.091667 0.157037 1 4105 tags = 40%, list = 19%, signal = 49% KEGG_JAK_STAT_SIGNALING_PATHWAY 125 −0.30333 −1.39847 0.014535 0.157726 1 2071 tags = 17%, list = 9%, signal = 18% NATSUME_RESPONSE_TO_INTERFERON_BETA_UP 60 −0.34866 −1.39702 0.027842 0.158946 1 2299 tags = 20%, list = 11%, signal = 22% MULLIGHAN_MLL_SIGNATURE_2_DN 222 −0.28409 −1.39699 0.003086 0.158673 1 3580 tags = 25%, list = 16%, signal = 29% GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_(—) 16 −0.49774 −1.39631 0.100877 0.159064 1 3226 tags = 44%, list = 15%, GREEN_UP signal = 51% AMIT_DELAYED_EARLY_GENES 17 −0.4758 −1.39595 0.112288 0.159133 1 4812 tags = 41%, list = 22%, signal = 53% DING_LUNG_CANCER_EXPRESSION_BY_COPY_NUMBER 87 −0.32447 −1.39372 0.019048 0.16113 1 7128 tags = 46%, list = 33%, signal = 68% LIU_CDX2_TARGETS_UP 34 −0.38811 −1.39227 0.072687 0.162389 1 1640 tags = 26%, list = 7%, signal = 29% KEGG_TYPE_I_DIABETES_MELLITUS 20 −0.44458 −1.39179 0.072527 0.162603 1 1967 tags = 30%, list = 9%, signal = 33% CROMER_TUMORIGENESIS_UP 40 −0.37638 −1.39164 0.058696 0.162456 1 4323 tags = 35%, list = 20%, signal = 44% DEURIG_T_CELL_PROLYMPHOCYTIC_LEUKEMIA_UP 283 −0.27378 −1.39152 0.008571 0.162236 1 6302 tags = 40%, list = 29%, signal = 56% HEIDENBLAD_AMPLICON_12P11_12_DN 20 −0.45761 −1.3913 0.084821 0.162175 1 4939 tags = 40%, list = 23%, signal = 52% OUYANG_PROSTATE_CANCER_PROGRESSION_DN 20 −0.44637 −1.3894 0.079007 0.163869 1 5543 tags = 50%, list = 25%, signal = 67% JAZAG_TGFB1_SIGNALING_UP 87 −0.32574 −1.38754 0.044554 0.165713 1 3619 tags = 25%, list = 17%, signal = 30% INGA_TP53_TARGETS 15 −0.4848 −1.38524 0.10101 0.167718 1 2331 tags = 40%, list = 11%, signal = 45% MANALO_HYPOXIA_UP 172 −0.29333 −1.3817 0.011561 0.171048 1 3766 tags = 28%, list = 17%, signal = 33% XU_HGF_SIGNALING_NOT_VIA_AKT1_48HR_DN 16 −0.48281 −1.38157 0.088795 0.170853 1 5908 tags = 63%, list = 27%, signal = 86% TURASHVILI_BREAST_LOBULAR_CARCINOMA_VS_(—) 69 −0.33538 −1.37992 0.039024 0.172203 1 294 tags = 10%, list = 1%, DUCTAL_NORMAL_DN signal = 10% NIKOLSKY_BREAST_CANCER_12Q13_Q21_AMPLICON 34 −0.3841 −1.37926 0.077803 0.172586 1 4173 tags = 32%, list = 19%, signal = 40% KEGG_ARGININE_AND_PROLINE_METABOLISM 47 −−0.3636 −1.37822 0.070776 0.173393 1 3132 tags = 30%, list = 14%, signal = 35% REACTOME_SYNTHESIS_OF_GLYCOSYLPHOSPHATIDYLINOSITOL 16 −0.47441 −1.37695 0.111588 0.174442 1 6172 tags = 44%, list = 28%, signal = 61% REACTOME_INACTIVATION_OF_APC_VIA_DIRECT_(—) 17 −0.46918 −1.37676 0.088838 0.174322 1 7138 tags = 53%, list = 33%, INHIBITION_OF_THE_APCOMPLEX signal = 78% ST_B_CELL_ANTIGEN_RECEPTOR 36 −0.38174 −1.37647 0.05814 0.17434 1 3812 tags = 28%, list = 17%, signal = 34% GAUSSMANN_MLL_AF4_FUSION_TARGETS_F_DN 27 −0.40752 −1.37623 0.095652 0.174294 1 2411 tags = 30%, list = 11%, signal = 33% KYNG_DNA_DAMAGE_BY_4NQO 17 −0.45897 −1.37587 0.107368 0.174363 1 1732 tags = 24%, list = 8%, signal = 26% SU_TESTIS 62 −0.34375 −1.37581 0.046683 0.174071 1 5348 tags = 42%, list = 24%, signal = 55% BROWNE_HCMV_INFECTION_2HR_UP 28 −0.407 −1.37524 0.08204 0.174391 1 3970 tags = 32%, list = 18%, signal = 39% REACTOME_UNFOLDED_PROTEIN_RESPONSE 18 −0.45886 −1.37523 0.115217 0.174075 1 7114 tags = 50%, list = 32%, signal = 74% IVANOVA_HEMATOPOIESIS_INTERMEDIATE_PROGENITOR 29 −0.41056 −1.37523 0.068522 0.173752 1 4404 tags = 41%, list = 20%, signal = 52% SENESE_HDAC1_TARGETS_UP 344 −0.26657 −1.37487 0 0.173825 1 5259 tags = 31%, list = 24%, signal = 40% KEGG_PRIMARY_IMMUNODEFICIENCY 35 −0.39068 −1.37478 0.077694 0.1736 1 3963 tags = 31%, list = 18%, signal = 38% AMIT_EGF_RESPONSE_60_MCF10A 33 −0.38962 −1.3747 0.070953 0.173354 1 4397 tags = 36%, list = 20%, signal = 45% MORI_PLASMA_CELL_UP 30 −0.40091 −1.3743 0.072562 0.17349 1 6311 tags = 43%, list = 29%, signal = 61% FERRANDO_T_ALL_WITH_MLL_ENL_FUSION_DN 67 −0.33108 −1.37238 0.029268 0.175255 1 6337 tags = 48%, list = 29%, signal = 67% DOANE_RESPONSE_TO_ANDROGEN_DN 203 −0.27826 −1.36984 0.011173 0.177593 1 3806 tags = 27%, list = 17%, signal = 32% SA_TRKA_RECEPTOR 15 −0.48644 −1.36971 0.108597 0.17744 1 1839 tags = 20%, list = 8%, signal = 22% YAMASHITA_LIVER_CANCER_WITH_EPCAM_UP 38 −0.37132 −1.36872 0.062791 0.178152 1 5931 tags = 29%, list = 27%, signal = 40% JAZAG_TGFB1_SIGNALING_VIA_SMAD4_DN 51 −0.35582 −1.36801 0.058685 0.178675 1 3297 tags = 24%, list = 15%, signal = 28% LIAO_METASTASIS 395 −0.26093 −1.36768 0 0.178704 1 4016 tags = 24%, list = 18%, signal = 29% CAIRO_HEPATOBLASTOMA_UP 172 −0.2862 −1.3674 0.00545 0.178707 1 5649 tags = 38%, list = 26%, signal = 51% HAHTOLA_SEZARY_SYNDROM_DN 32 −0.39169 −1.36721 0.084071 0.178597 1 1716 tags = 22%, list = 8%, signal = 24% PROVENZANI_METASTASIS_UP 153 −0.29047 −1.3665 0.002849 0.179207 1 4855 tags = 27%, list = 22%, signal = 34% REACTOME_SIGNALLING_TO_ERKS 32 −0.39226 −1.36647 0.091981 0.178911 1 5189 tags = 22%, list = 24%, signal = 29% KEGG_OXIDATIVE_PHOSPHORYLATION 105 −0.30522 −1.36542 0.019753 0.179829 1 9520 tags = 50%, list = 43%, signal = 87% NIKOLSKY_BREAST_CANCER_6P24_P22_AMPLICON 16 −0.45905 −1.36526 0.111111 0.179648 1 1518 tags = 19%, list = 7%, signal = 20% REACTOME_CENTROSOME_MATURATION 59 −0.34139 −1.36439 0.042254 0.18028 1 7600 tags = 44%, list = 35%, signal = 67% GAUSSMANN_MLL_AF4_FUSION_TARGETS_G_DN 27 −0.4069 −1.36369 0.089862 0.18075 1 3580 tags = 33%, list = 16%, signal = 40% REACTOME_ELECTRON_TRANSPORT_CHAIN 60 −0.34238 −1.36326 0.048055 0.1809 1 9617 tags = 52%, list = 44%, signal = 92% PUIFFE_INVASION_INHIBITED_BY_ASCITES_UP 62 −0.33929 −1.36065 0.053528 0.183487 1 7069 tags = 52%, list = 32%, signal = 76% ALCALAY_AML_BY_NPM1_LOCALIZATION_DN 160 −0.29008 −1.35956 0.020231 0.184411 1 5407 tags = 39%, list = 25%, signal = 51% REACTOME_DOWNSTREAM_SIGNALING_OF_ACTIVATED_(—) 41 −0.3687 −1.35949 0.073394 0.18419 1 2299 tags = 20%, list = 11%, FGFR signal = 22% GRADE_COLON_VS_RECTAL_CANCER_DN 35 −0.38706 −1.3576 0.092511 0.186036 1 2486 tags = 26%, list = 11%, signal = 29% REACTOME_ZINC_TRANSPORTATION 17 −0.46026 −1.35645 0.112527 0.187041 1 6501 tags = 65%, list = 30%, signal = 92% REACTOME_CHEMOKINE_RECEPTORS_BIND_CHEMOKINES 44 −0.36558 −1.35641 0.069378 0.186759 1 561 tags = 18%, list = 3%, signal = 19% NOUZOVA_TRETINOIN_AND_H4_ACETYLATION 97 −0.31025 −1.35591 0.024691 0.186986 1 6672 tags = 43%, list = 30%, signal = 62% PUIFFE_INVASION_INHIBITED_BY_ASCITES_DN 113 −0.29756 −1.35527 0.032663 0.187369 1 5450 tags = 29%, list = 25%, signal = 39% IZADPANAH_STEM_CELL_ADIPOSE_VS_BONE_UP 92 −0.31369 −1.35476 0.041995 0.187571 1 1854 tags = 18%, list = 8%, signal = 20% BERENJENO_TRANSFORMED_BY_RHOA_REVERSIBLY_(—) 28 −0.40651 −1.35346 0.084071 0.188776 1 4723 tags = 43%, list = 22%, DN signal = 55% RUGO_RESPONSE_TO_4NQO 17 −0.45897 −1.35286 0.121413 0.189087 1 1732 tags = 24%, list = 8%, signal = 26% ZHAN_V2_LATE_DIFFERENTIATION_GENES 30 −0.39762 −1.35079 0.110855 0.191172 1 829 tags = 13%, list = 4%, signal = 14% KEGG_BLADDER_CANCER 37 −0.37393 −1.3502 0.083732 0.191564 1 3471 tags = 30%, list = 16%, signal = 35% AMIT_SERUM_RESPONSE_40_MCF10A 26 −0.4153 −1.34967 0.083333 0.19181 1 3857 tags = 38%, list = 18%, signal = 47% BASSO_B_LYMPHOCYTE_NETWORK 117 −0.29903 −1.34907 0.026455 0.192131 1 5766 tags = 41%, list = 26%, signal = 55% KEGG_GAP_JUNCTION 72 −0.31987 −1.34898 0.057292 0.191883 1 5612 tags = 31%, list = 26%, signal = 41% DAIRKEE_CANCER_PRONE_RESPONSE_BPA 42 −0.36551 −1.34701 0.084706 0.193933 1 6558 tags = 45%, list = 30%, signal = 64% ZHAN_MULTIPLE_MYELOMA_UP 45 −0.35975 −1.34516 0.068027 0.195909 1 3138 tags = 22%, list = 14%, signal = 26% GARGALOVIC_RESPONSE_TO_OXIDIZED_PHOSPHOLIPIDS_(—) 20 −0.43645 −1.34499 0.105376 0.195757 1 4644 tags = 35%, list = 21%, GREEN_DN signal = 44% LI_AMPLIFIED_IN_LUNG_CANCER 151 −0.28645 −1.34477 0.032967 0.19569 1 6606 tags = 36%, list = 30%, signal = 51% NIKOLSKY_BREAST_CANCER_16P13_AMPLICON 80 −0.31761 −1.34287 0.041775 0.197573 1 6234 tags = 35%, list = 28%, signal = 49% DORN_ADENOVIRUS_INFECTION_12HR_DN 25 −0.41072 −1.33962 0.115473 0.201171 1 2099 tags = 24%, list = 10%, signal = 27% MATTIOLI_MGUS_VS_PCL 80 −0.31539 −1.33921 0.045685 0.20132 1 8124 tags = 59%, list = 37%, signal = 93% BROWNE_HCMV_INFECTION_48HR_UP 152 −0.28689 −1.33802 0.021918 0.202463 1 3838 tags = 26%, list = 18%, signal = 31% REACTOME_METAL_ION_SLC_TRANSPORTERS 23 −0.41626 −1.33738 0.113527 0.202874 1 6501 tags = 57%, list = 30%, signal = 80% KEGG_FRUCTOSE_AND_MANNOSE_METABOLISM 31 −0.38665 −1.33501 0.095794 0.205558 1 3136 tags = 29%, list = 14%, signal = 34% ALONSO_METASTASIS_EMT_UP 28 −0.39044 −1.3334 0.104019 0.207212 1 5944 tags = 46%, list = 27%, signal = 64% GAZDA_DIAMOND_BLACKFAN_ANEMIA_MYELOID_UP 24 −0.40873 −1.33216 0.120879 0.208481 1 4222 tags = 38%, list = 19%, signal = 46% DAZARD_RESPONSE_TO_UV_NHEK_UP 131 −0.28972 −1.33138 0.032 0.209178 1 3553 tags = 24%, list = 16%, signal = 29% BROCKE_APOPTOSIS_REVERSED_BY_IL6 114 −0.29444 −1.33029 0.032609 0.210268 1 6301 tags = 41%, list = 29%, signal = 58% BARIS_THYROID_CANCER_DN 52 −0.34946 −1.33019 0.070707 0.210052 1 4070 tags = 23%, list = 19%, signal = 28% WOOD_EBV_EBNA1_TARGETS_UP 98 −0.30448 −1.32962 0.059896 0.210401 1 3669 tags = 28%, list = 17%, signal = 33% REACTOME_TIGHT_JUNCTION_INTERACTIONS 28 −0.38824 −1.32925 0.10274 0.210475 1 3920 tags = 36%, list = 18%, signal = 43% REACTOME_REGULATION_OF_ORNITHINE_DECARBOXYLASE 46 −0.35349 −1.32563 0.09828 0.214739 1 8423 tags = 63%, list = 38%, signal = 102% GALLUZZI_PERMEABILIZE_MITOCHONDRIA 35 −0.36982 −1.32513 0.091723 0.214976 1 6001 tags = 49%, list = 27%, signal = 67% YAO_TEMPORAL_RESPONSE_TO_PROGESTERONE_(—) 15 −0.46388 −1.32412 0.137778 0.215918 1 4888 tags = 47%, list = 22%, CLUSTER_4 signal = 60% BENPORATH_ES_CORE_NINE_CORRELATED 91 −0.30699 −1.32391 0.035806 0.21583 1 6570 tags = 43%, list = 30%, signal = 61% KEGG_UBIQUITIN_MEDIATED_PROTEOLYSIS 118 −0.296 −1.32145 0.033241 0.218606 1 6495 tags = 36%, list = 30%, signal = 52% TANAKA_METHYLATED_IN_ESOPHAGEAL_CARCINOMA 75 −0.31873 −1.32092 0.065823 0.218944 1 4644 tags = 32%, list = 21%, signal = 40% RUGO_RESPONSE_TO_GAMMA_RADIATION 39 −0.36072 −1.32014 0.098558 0.219606 1 1156 tags = 15%, list = 5%, signal = 16% XU_HGF_SIGNALING_NOT_VIA_AKT1_6HR 22 −0.42546 −1.31901 0.129386 0.220615 1 4729 tags = 45%, list = 22%, signal = 58% WATTEL_AUTONOMOUS_THYROID_ADENOMA_UP 18 −0.43983 −1.31832 0.138144 0.221187 1 2366 tags = 33%, list = 11%, signal = 37% ENK_UV_RESPONSE_EPIDERMIS_DN 439 −0.24798 −1.31748 0.003802 0.221869 1 4819 tags = 28%, list = 22%, signal = 35% REACTOME_IRS_RELATED_EVENTS 71 −0.32099 −1.31736 0.054502 0.22169 1 2338 tags = 17%, list = 11%, signal = 19% CREIGHTON_ENDOCRINE_THERAPY_RESISTANCE_1 388 −0.25131 −1.31344 0.006757 0.226775 1 5469 tags = 32%, list = 25%, signal = 43% OUELLET_OVARIAN_CANCER_INVASIVE_VS_LMP_UP 105 −0.29715 −1.31312 0.053571 0.226785 1 7051 tags = 42%, list = 32%, signal = 62% BIOCARTA_BAD_PATHWAY 24 −0.40186 −1.31268 0.121593 0.226992 1 1346 tags = 13%, list = 6%, signal = 13% REACTOME_SYNTHESIS_AND_INTERCONVERSION_OF_(—) 16 −0.45318 −1.31235 0.145089 0.227095 1 6525 tags = 63%, list = 30%, NUCLEOTIDE_DI_AND_TRIPHOSPHATES signal = 89% WANG_CISPLATIN_RESPONSE_AND_XPC_UP 106 −0.29389 −1.31204 0.052219 0.227107 1 5908 tags = 36%, list = 27%, signal = 49% REACTOME_FURTHER_PLATELET_RELEASATE 20 −0.4288 −1.31183 0.12065 0.227023 1 196 tags = 10%, list = 1%, signal = 10% FLOTHO_PEDIATRIC_ALL_THERAPY_RESPONSE_DN 20 −0.43318 −1.31001 0.147609 0.22914 1 3841 tags = 45%, list = 18%, signal = 55% HAMAI_APOPTOSIS_VIA_TRAIL_UP 292 −0.25561 −1.30972 0.006349 0.229122 1 4889 tags = 30%, list = 22%, signal = 38% REACTOME_PHOSPHORYLATION_OF_THE_APC 15 −0.46234 −1.30877 0.120879 0.22999 1 7138 tags = 53%, list = 33%, signal = 79% MULLIGHAN_NPM1_MUTATED_SIGNATURE_1_UP 211 −0.26002 −1.30758 0.012232 0.231218 1 5047 tags = 29%, list = 23%, signal = 38% SWEET_LUNG_CANCER_KRAS_UP 442 −0.24403 −1.30611 0.00365 0.232909 1 4747 tags = 24%, list = 22%, signal = 30% KYNG_DNA_DAMAGE_BY_GAMMA_RADIATION 39 −0.36072 −1.30513 0.123543 0.233851 1 1156 tags = 15%, list = 5%, signal = 16% SHAFFER_IRF4_MULTIPLE_MYELOMA_PROGRAM 35 −0.37016 −1.3046 0.10643 0.234189 1 6001 tags = 49%, list = 27%, signal = 67% BIOCARTA_PTDINS_PATHWAY 22 −0.41198 −1.30389 0.115294 0.234737 1 2241 tags = 14%, list = 10%, signal = 15% RICKMAN_TUMOR_DIFFERENTIATED_WELL_VS_POORLY_(—) 175 −0.27162 −1.30354 0.027933 0.234776 1 5781 tags = 36%, list = 26%, UP signal = 49% CUI_TCF21_TARGETS_DN 31 −0.37395 −1.30352 0.107623 0.234418 1 3639 tags = 39%, list = 17%, signal = 46% JI_RESPONSE_TO_FSH_DN 44 −0.33997 −1.3032 0.098214 0.234476 1 3310 tags = 23%, list = 15%, signal = 27% CAIRO_LIVER_DEVELOPMENT_UP 143 −0.27913 −1.30278 0.025707 0.234671 1 4590 tags = 29%, list = 21%, signal = 37% REACTOME_BRANCHED_CHAIN_AMINO_ACID_CATABOLISM 16 −0.44355 −1.30278 0.1566 0.234293 1 4842 tags = 38%, list = 22%, signal = 48% REACTOME_PYRUVATE_METABOLISM 15 −0.46909 −1.29992 0.16309 0.238032 1 7030 tags = 60%, list = 32%, signal = 88% WINTER_HYPOXIA_METAGENE 190 −0.26745 −1.29969 0.017391 0.237964 1 3203 tags = 23%, list = 15%, signal = 26% CHESLER_BRAIN_QTL_CIS 68 −0.31806 −1.29925 0.071253 0.238215 1 4520 tags = 29%, list = 21%, signal = 37% AIGNER_ZEB1_TARGETS 28 −0.38265 −1.29922 0.124711 0.237876 1 1207 tags = 21%, list = 6%, signal = 23% KYNG_DNA_DAMAGE_UP 89 −0.30141 −1.29871 0.082915 0.238145 1 2200 tags = 18%, list = 10%, signal = 20% WU_APOPTOSIS_BY_CDKN1A_VIA_TP53 28 −0.39139 −1.29864 0.138158 0.237897 1 6063 tags = 57%, list = 28%, signal = 79% SESTO_RESPONSE_TO_UV_C0 95 −0.30145 −1.29724 0.058824 0.23949 1 8116 tags = 47%, list = 37%, signal = 75% KEGG_PEROXISOME 68 −0.30916 −1.29473 0.070423 0.242697 1 4526 tags = 32%, list = 21%, signal = 41% MARKEY_RB1_CHRONIC_LOF_UP 106 −0.29214 −1.29443 0.045802 0.242773 1 7461 tags = 51%, list = 34%, signal = 77% SHI_SPARC_TARGETS_UP 19 −0.41989 −1.29379 0.129464 0.24335 1 2615 tags = 26%, list = 12%, signal = 30% REACTOME_GLUCONEOGENESIS 26 −0.39437 −1.29324 0.125275 0.243803 1 4616 tags = 35%, list = 21%, signal = 44% REACTOME_DOWN_STREAM_SIGNAL_TRANSDUCTION 35 −0.35619 −1.29187 0.113043 0.245395 1 1359 tags = 9%, list = 6%, signal = 9% AMUNDSON_POOR_SURVIVAL_AFTER_GAMMA_RADIATION_(—) 127 −0.28342 −1.29163 0.033613 0.245292 1 4962 tags = 30%, list = 23%, 2G signal = 38%

TABLE 3 p value Foxp3Cre Nrp1 f/f x Foxp3 Cre Gene Symbol Gene Title (interaction) Sema/IgG Sema/IgG Pf4 platelet factor 4 0.00009599 1.545577742 1.009665494 Ntn4 netrin 4 0.00000305 1.352296007 1.172896253 Gbp1 guanylate binding protein 1 6.342E−12 1.355007012 1.16096399 Sox6 SRY-box containing gene 6 0.0030674 1.443495801 0.972584119 Zbtb20 zinc finger and BTB domain containing 20 0.000001211 1.331835698 1.082126493 Zbtb4 zinc finger and BTB domain containing 4  3.64E−09 1.255748611 1.082036273 S1pr1 sphingosine-1-phosphate receptor 1 2.009E−09 1.204529765 1.087154433 Selp selectin, platelet 0.00203095 1.300955862 1.043575103 Klf2 Kruppel-like factor 2 (lung) 3.671E−10 1.285134665 1.106060488 Capn3 calpain 3 0.0108324 1.269066665 1.041143567 P2rx7 purinergic receptor P2X, ligand-gated ion channel, 7 2.507E−09 1.254283105 1.062555789 Trat1 T cell receptor associated transmembrane adaptor 1 2.002E−08 1.247496664 1.115014034 Klf3 Kruppel-like factor 3 (basic) 5.206E−08 1.242062467 1.097946279 Irf7 interferon regulatory factor 7 0.00003947 1.237559009 0.966178546 Sox4 SRY-box containing gene 4 0.00026928 1.218840832 1.069164455 Socs3 suppressor of cytokine signaling 3 0.000002704 1.197338018 1.043479784 Ccr2 chemokine (C-C motif) receptor 2 0.00088497 1.194479665 0.944542178 Cd86 CD86 antigen 0.00095436 1.15990739 1.030515958 Csf1 colony stimulating factor 1 (macrophage) 0.00018162 1.139043688 0.983451169 Tnfrsf22 tumor necrosis factor receptor superfamily, member 22 0.029579 1.135265234 0.999410833 Sele selectin, endothelial cell 0.0611511 1.126037378 0.944445866 Bcl2 B-cell leukemia/lymphoma 2 0.000001345 1.200530854 1.036517252 Ikzf2 IKAROS family zinc finger 2 0.00539308 1.107958566 1.029981749 Gpr83 G protein-coupled receptor 83 7.928E−08 1.103769744 1.035679639 Nt5e 5′ nucleotidase, ecto 7.126E−11 1.115728599 1.042848886 Pias1 protein inhibitor of activated STAT 1 7.054E−07 1.229350664 1.051712288 Pde2a phosphodiesterase 2A, cGMP-stimulated 7.143E−07 1.220384964 1.136825712 Samhd1 SAM domain and HD domain, 1 8.458E−08 1.272371694 1.088937279 Rasgrp1 RAS guanyl releasing protein 1 8.266E−10 1.132277662 1.052465539 Sell selectin, lymphocyte 1.864E−08 1.119421504 1.040753113 Ifngr1 interferon gamma receptor 1 8.769E−10 1.139298486 1.054594449 Il6st interleukin 6 signal transducer 3.242E−08 1.124112682 1.034980857 Socs2 suppressor of cytokine signaling 2 0.0013229 1.165949171 1.089333063 Klrc1 killer cell lectin-like receptor subfamily C, member 1 0.0231404 0.839384892 0.958292103 Il4 interleukin 4 0.0456394 0.884948909 0.98797694 Il5 interleukin 5 0.0200249 0.866258511 0.967564087 Il17a interleukin 17A 0.0892365 0.876784798 0.980557686 Irf4 interferon regulatory factor 4 0.00166111 0.865581808 0.914790588 Irf8 interferon regulatory factor 8 1.627E−07 0.815320769 0.902639353 Casp3 caspase 3 0.00101569 0.768470287 0.986386473 Lag3 lymphocyte-activation gene 3 0.00074161 0.81582849 0.989058591 Pax3 paired box gene 3 0.0100615 0.824486955 1.028467901 Rorc RAR-related orphan receptor gamma 0.0478239 0.82459593 1.058781462 Eomes eomesodermin homolog (Xenopus laevis) 0.00329137 0.825853154 0.958256158 Il9 interleukin 9 0.0597995 0.83668632 0.99566111 Klf1 Kruppel-like factor 1 (erythroid) 0.00007452 0.845474592 1.076712711 Il17re interleukin 17 receptor E 0.037236 0.886991987 1.012299813 Bcl7c B-cell CLL/lymphoma 7C 0.000004747 0.894221815 1.066003659 Alcam activated leukocyte cell adhesion molecule 0.0031076 0.793324239 0.957458743 Nedd4 neural precursor cell expressed, developmentally down-regulated 4 0.000002309 0.807636853 1.058385025 Vegfc vascular endothelial growth factor C 0.00171023 0.769523371 1.052111027 Spry2 sprouty homolog 2 (Drosophila) 0.00029642 0.760398934 0.91800687 Rgs16 regulator of G-protein signaling 16 0.00002906 0.77611906 0.915180984 Serpine2 serine (or cysteine) peptidase inhibitor, clade E, member 2 3.332E−09 0.69502868 0.83449972 Bcat1 branched chain aminotransferase 1, cytosolic 0.000004398 0.737455065 0.96648127 Pdgfb platelet derived growth factor, B polypeptide 0.00004784 0.656164641 0.857934741 Il3 interleukin 3 0.00004922 0.594682398 0.78279364 

1-116. (canceled)
 117. A pharmaceutical composition comprising an isolated anti-neuropilin-1 (NRP-1) antibody specific for cell surface NRP-1, wherein the anti-NRP-1 antibody is present in the composition in an amount effective to inhibit an interaction between NRP-1 and a transmembrane semaphorin-4 polypeptide when administered to a human subject.
 118. The pharmaceutical composition of claim 117, wherein the anti-NRP-1 antibody does not affect the interaction between a NRP-1 polypeptide and a vascular endothelial growth factor (VEGF) polypeptide.
 119. The pharmaceutical composition of claim 117, wherein the anti-NRP-1 antibody is capable of inhibiting Treg suppression in the human subject.
 120. The pharmaceutical composition of claim 117, wherein the anti-NRP-1 antibody is capable of decreasing Treg survival and/or stability in the human subject.
 121. The pharmaceutical composition of claim 117, wherein the anti-NRP-1 antibody is present in the composition in an amount effective to locally inhibit the NRP-1:semaphorin-4 interaction in a tumor.
 122. The pharmaceutical composition of claim 117, wherein the anti-NRP-1 antibody is present in the composition in an amount effective to prevent development of an undesired autoimmune and/or inflammatory manifestation.
 123. The pharmaceutical composition of claim 117, wherein the human subject is suffering from a cancer.
 124. The pharmaceutical composition of claim 117, wherein the anti-NRP-1 antibody specifically binds to an epitope that is bound by a transmembrane semaphorin-4 polypeptide.
 125. The pharmaceutical composition of claim 117, wherein the inhibition of the NRP-1:semaphorin-4 interaction is demonstrated using an in vitro transwell suppression assay.
 126. The pharmaceutical composition of claim 117, wherein the transmembrane semaphorin-4 polypeptide consists of a transmembrane semaphorin-4A polypeptide.
 127. An isolated nucleic acid or nucleic acids that encode the anti-NRP-1 antibody present in the pharmaceutical composition of claim
 117. 128. A method of inhibiting a function or decreasing stability of a regulatory T cell (Treg) comprising exposing the Treg in vivo to an inhibitor of neuropilin-1 (Nrp1):semaphorin-4 axis in the Treg, wherein the inhibitor comprises an anti-NRP-1 antibody.
 129. The method of claim 128, wherein the anti-NRP-1 antibody inhibits interaction between i) a transmembrane semaphorin-4 polypeptide on a cell expressing the transmembrane semaphorin-4 and ii) a NRP-1 polypeptide on the Treg.
 130. The method of claim 129, wherein the cell expressing the transmembrane semaphorin-4 is selected from the group consisting of a conventional T cell, a conventional dendritic cell, and a plasmacytoid dendritic cell.
 131. The method of claim 128, comprising administering to a human subject suffering from a cancer a pharmaceutical composition comprising an effective amount of the anti-NRP-1 antibody.
 132. The method of claim 128, wherein the anti-NRP-1 antibody is capable of decreasing Treg survival and/or stability in the human subject.
 133. The method of claim 128, wherein the anti-NRP-1 antibody is capable of binding to an extracellular domain of the NRP-1 polypeptide.
 134. A method of treating cancer in a human subject in need thereof, the method comprising the step of inhibiting a neuropilin-1 (Nrp1):semaphorin-4 axis in regulatory T cells (Tregs) of the subject, wherein the neuropilin-1 (Nrp1):semaphorin-4 axis is inhibited by administration to the human subject of a pharmaceutical composition comprising an anti-NRP-1 antibody, thereby treating the cancer.
 135. The method of claim 134, wherein the anti-NRP-1 antibody does not affect the interaction between a NRP-1 polypeptide and a vascular endothelial growth factor (VEGF) polypeptide.
 136. The method of claim 134, wherein the anti-NRP-1 antibody increases Akt phosphorylation. 